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clinical trials research assistant or associate pediatrics endocrine diabetes

University of Iowa

<div>
 Within the Stead Family Department of Pediatrics, Division of Endocrinology, we seek to hire a full time Clinical Trials Research Assistant (PRV1) or Clinical Trials Research Associate (PRV2). This position will provide support for Pediatric Endocrinology and Diabetes Clinical Research by conducting study visits, collecting and analyzing results and performing operational duties associated with human research.
 <strong>
  This is a specified term position.
  <br/>
  <br/>
 </strong>
 <em>
  The Division of Endocrinology intends to hire either a Clinical Trials Research Assistant (PRV1) or a Clinical Trials Research Associate (PRV2), based on the qualifications of the successful candidate. Please indicate in your application materials the position you wish to be considered for or indicate both.
  <br/>
  <br/>
 </em>
 <em>
  <strong>
   Pay Level:
  </strong>
  3A (PRV1) or 4A (PRV2)
  <br/>
  <br/>
 </em>
 <strong>
  Full job descriptions for both positions can be obtained by emailing pedsuichildrenshr@healthcare.uiowa.edu.
  <br/>
  <br/>
 </strong>
 Primary responsibilities of the Clinical Trials Research Assistant (PRV1; 3A) include:
 <br/>
 <br/>
 <ul>
  <li>
   Perform research activities in a specialized area.
  </li>
  <li>
   Consult with principal investigator to design forms to facilitate the collection and tracking of participant data, study drugs and study procedures. Design study source documents, assessment tools, and participant questionnaires.
  </li>
  <li>
   Meet with families to introduce them to research opportunities currently available.
  </li>
  <li>
   Perform procedures and techniques as outlined in clinical research protocols, assure fidelity to protocols.
  </li>
  <li>
   Complete basic lab processing, sample storage and lab shipments per protocol.
  </li>
  <li>
   Use statistical analysis software (REDCap) to analyze and summarize study data.
  </li>
  <li>
   Submit protocols to the IRB and other review committees for approval prior to implementing research, as necessary for modifications and then annually for continuing review approvals.
  </li>
  <li>
   Responsible for safety programs by following guidelines and maintaining required documentation. Document all participant Serious Adverse Events and Adverse Events and report these to the primary investigator, study sponsor, and IRB.
  </li>
  <li>
   Attend local and national research meetings as required. Present results, findings or updates.
  </li>
  <li>
   Attend local fundraising events and activities to market and recruit participants for research studies.
  </li>
  <li>
   Conduct routine maintenance and controls on continuous glucose monitoring devices, glucose meters, YSI analyzer, and centrifuge.
  </li>
  <li>
   Participate in managing the student research staff to ensure task completion and compliance with UI policies and procedures. Provide directions, assignments, feedback, coaching and counseling to ensure outcomes are achieved. Provide training and oversight on basic lab requirements and protocols.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Primary responsibilities of the Clinical Trials Research Assistant (PRV2; 4A) include:
 <br/>
 <br/>
 <ul>
  <li>
   Perform research activities in a specialized area.
  </li>
  <li>
   Assist in the design, development, execution administration and maintenance of protocols and clinical studies. Assist in study design and protocol development and provide input into descriptions of complex research procedures.
  </li>
  <li>
   Consult with principal investigator to design forms to facilitate the collection and tracking of participant data, study drugs and study procedures.
  </li>
  <li>
   Oversee the recruitment of subjects and scheduling of trial-related procedures.
  </li>
  <li>
   Meet with families to introduce them to research opportunities currently available. Responsible for subject recruitment, subject management, scheduling, phone calls, etc. to aid in coordination of study visits.
  </li>
  <li>
   Perform procedures and techniques as outlined in clinical research protocols, assure fidelity to protocols. Download insulin pumps and glucose meters; assist with tolerance tests, clamp studies, and other procedures.
  </li>
  <li>
   Participate in the design, development, and testing of clinical research trials data systems. Validate data, query resolution, and make recommendations for resolution. Revise and implement change in data collection.
  </li>
  <li>
   Use statistical analysis software (REDCap) to analyze and summarize study data.
  </li>
  <li>
   Submit protocols to the IRB and other review committees for approval prior to implementing research.
  </li>
  <li>
   Responsible for safety programs by following guidelines and maintaining required documentation. Document all participant Serious Adverse Events and Adverse Events and report these to the primary investigator, study sponsor, and IRB.
  </li>
  <li>
   Monitor implementation of study per protocol and ensure procedures are conducted using good clinical practice standards and meeting IRB guidelines.
  </li>
  <li>
   Manage and organize regulatory documentation from sites and regulatory authorities. Prepare regulatory submissions. Perform on-site audits of research and clinical data.
  </li>
  <li>
   Collaborate with Study Sponsors and Coordinating Centers to manage protocols. Meet with study monitors as requested.
  </li>
  <li>
   Attend local and national research meetings as required. Present results, findings or updates.
  </li>
  <li>
   Attend local fundraising events and activities to market and recruit participants for research studies.
  </li>
  <li>
   Conduct routine maintenance and controls on continuous glucose monitoring devices, glucose meters, YSI analyzer, and centrifuge. Manage study equipment to ensure safety of study participants and monitor environmental risks.
  </li>
  <li>
   Coordinate, manage and test equipment. Troubleshoot and resolve equipment failures, error codes and repairs.
  </li>
  <li>
   Participate in managing the research staff to assure task completion and compliance with UI policies and procedures. Provide direction, assignments, feedback, coaching and counseling to ensure outcomes are achieved. Provide training and oversight into basic lab requirements and protocols.
  </li>
  <li>
   May provide functional and/or administrative supervision. Mentor new staff under direction.
  </li>
  <li>
   Assist in preparing budgets for studies and timely billing compliance for studies.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Education Requirements
   <br/>
   <br/>
  </strong>
 </strong>
 <strong>
  CLINICAL TRIALS RESEARCH ASSISTANT (PRV1) REQUIRED QUALIFICATIONS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s Degree in related field or an equivalency of education and/or related experience.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Experience Requirements
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Excellent written, verbal and interpersonal communication skills.
  </li>
  <li>
   Demonstrated proficiency with Microsoft Office and software applications, and ability to learn new applications or systems.
  </li>
  <li>
   Experience working independently and in a group setting.
  </li>
  <li>
   Experience managing information requiring attention to detail and high level of organization.
  </li>
  <li>
   Experience with data entry and management.
  </li>
  <li>
   Minimum 6 months of research experience
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Highly Desired Qualifications
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Experience in medical or clinical research directly related to endocrinology and diabetes.
  </li>
  <li>
   Demonstrated ability to multi-task and excellent time management skills.
  </li>
  <li>
   Knowledge of medical terminology related to pediatric endocrinology and diabetes.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Education Requirements
   <br/>
   <br/>
  </strong>
 </strong>
 <strong>
  CLINICAL TRIALS RESEARCH ASSOCIATE (PRV2) REQUIRED QUALIFICATIONS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A Bachelor&rsquo;s Degree in a related field or an equivalency of education and/or related experience.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Experience Requirements
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Excellent written, verbal and interpersonal communication skills.
  </li>
  <li>
   Demonstrated proficiency with Microsoft Office and software applications, and ability to learn new applications or systems.
  </li>
  <li>
   Experience working independently and in a group setting.
  </li>
  <li>
   Experience managing information requiring attention to detail and high level of organization.
  </li>
  <li>
   Experience with data entry and management.
  </li>
  <li>
   Minimum of 1 year of research experience.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Position And Application Details:
   <br/>
   <br/>
  </strong>
 </strong>
 In order to be considered for an interview, applicants must upload the following documents and mark them as a &ldquo;Relevant File&rdquo; to the submission:
 <br/>
 <br/>
 <ul>
  <li>
   Resume
  </li>
  <li>
   Cover Letter
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.
 <br/>
 <br/>
 Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.
 <br/>
 <br/>
 For additional questions, please contact pedsuichildrenshr@healthcare.uiowa.edu
 <br/>
 <br/>
 <strong>
  This position is not eligible for university sponsorship for employment authorization.
  <br/>
  <br/>
 </strong>
 Additional Information
 <br/>
 <br/>
 <ul>
  <li>
   Classification Title: Clin Trials Rsrch Associate
  </li>
  <li>
   Appointment Type: Professional and Scientific
  </li>
  <li>
   Schedule: Full-time
  </li>
  <li>
   Work Modality Options: On Campus
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compensation
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Pay Level: 4A
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Contact Information
 <br/>
 <br/>
 <ul>
  <li>
   Organization: Healthcare
  </li>
  <li>
   Contact Name: Pediatric Human Resources
  </li>
  <li>
   Contact Email: Pedsuichildrenshr@healthcare.uiowa.edu
  </li>
 </ul>
</div>


Clinical Trials Research Assistant or Associate - Pediatrics Endocrine & Diabetes

<div>
 BASIC FUNCTION AND RESPONSIBILITY
 <br/>
 <br/>
 Function as a Physician Assistant and change agent incorporating the primary role of PA and the supporting roles of consultant, educator, researcher, and administrator to support quality care and positive patient outcomes for the Weight Management Clinic. This growing outpatient practice incorporates a multidisciplinary approach to patient care involving physicians, mid-level providers, dieticians, and certified diabetes educators to treat patients with obesity. The successful candidate will be expected to manage a panel of patients independently as well as work with the multidisciplinary team in a shared care model.
 <br/>
 <br/>
 <strong>
  Characteristic Duties And Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assure clinical competency and expertise in areas of weight management, endocrinology and diabetes.
  </li>
  <li>
   Function independently and/or as a member of an interdisciplinary team to plan, deliver and evaluate health care for patients with weight management, diabetes and endocrine diseases.
  </li>
  <li>
   Collaborate with nursing staff/nursing administration to monitor and evaluate the quality of patient care.
  </li>
  <li>
   Determine nursing care requirements and develop programs for weight management, endocrine/diabetes patients, with regard to patient condition and ag and follow universal precautions.
  </li>
  <li>
   Promote health maintenance that spans the continuum of health from outpatient to inpatient settings and back to the home care arena.
  </li>
  <li>
   Perform medical diagnostic, therapeutic procedures, and prescribe, dispense or deliver medications when a collaborative practice agreement is in place.
  </li>
  <li>
   Provide anticipatory guidance and counseling to patients/families.
  </li>
  <li>
   Document patient assessment and plan of care in the medical record and generate appropriate health reports for outgoing correspondence.
  </li>
  <li>
   Initiate and coordinate referrals to other healthcare team members or agencies.
  </li>
  <li>
   Serve in a consultative resource capacity by providing expert knowledge and behavioral skills that impact clinical practice and patient outcomes.
  </li>
  <li>
   Participate in the development, utilization and evaluation of resources to meet patient/family educational needs.
  </li>
  <li>
   Provide education and serve as a resource for nursing staff in area of clinical expertise.
  </li>
  <li>
   Provide education to external agencies, community and other health professionals.
  </li>
  <li>
   Generate research questions regarding health care for particular patient populations.
  </li>
  <li>
   Incorporate research findings into practice.
  </li>
  <li>
   Participate in the development and implementation of divisional and departmental quality assessment/improvement/research programs and processes.
  </li>
  <li>
   Responsible for administrative activities and special projects as assigned.
  </li>
  <li>
   Contribute toward the achievement of divisional and departmental goals.
  </li>
  <li>
   Participate and contribute to activities that enhance clinical expertise and nursing knowledge.
  </li>
  <li>
   Participate in professional nursing activities in the department, hospital, community, and professional organizations.
  </li>
  <li>
   Instruct and counsel patients regarding physical and mental health on matters such as diets, disease, therapy, and normal growth and development.
  </li>
  <li>
   Assist in the delivery of services to patients requiring continuing care.
  </li>
  <li>
   Maintain effective working relationships with faculty, staff, students, and the public.
  </li>
  <li>
   Establish and maintain standards of collaborative interaction among peers and employees that is characterized by respect, honesty and service; assure that all unit members are held to similar standards and ethics; constructively manages conflict.
  </li>
  <li>
   Inspire and motivate others to high performance by exercising strong stewardship of University resources, setting expectations, measuring success through individual performance evaluations, and driving organizational results.
  </li>
  <li>
   Identify opportunities for and creates development plans that encourage employees to attend to the growth of their personal and professional capacity; engage self and staff in collective reflection of the University&rsquo;s greater role in society.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  The department intends to hire for one position as either an ARNP, requisition 25005808 or PA, requisition 25005809, based on the qualifications of the successful candidate. Please apply to the specific position for which you which to be considered or both.
  <br/>
  <br/>
 </strong>
 <strong>
  Education Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Must comply with registration and licensure requirements as specified by the Iowa Board of Physician Assistant Examiners which include graduation from an accredited PA educational program and/or certification by the NCCPA.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Excellent written and verbal communication skills are required.
  </li>
  <li>
   Demonstrated experience in the area of clinical practice is required.
  </li>
  <li>
   Experience in the area of weight management is highly desirable.
  </li>
  <li>
   Experience in the area of diabetes is highly desirable.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 CLINICAL EXPECTATIONS
 <br/>
 <br/>
 <ul>
  <li>
   8 half-days per week in the Weight Management outpatient clinic in various UI Health Care locations and telehealth. Clinics are likely to be scheduled Monday-Friday in the morning, afternoon, or evening; however, Saturday clinics may be needed if clinic space is not available.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Position and Application Details
 <br/>
 <br/>
 In Order To Be Considered For An Interview, Applicants Must Upload The Following Documents And Mark Them As a &ldquo;Relevant File&rdquo; To The Submission
 <br/>
 <br/>
 <ul>
  <li>
   Resume
  </li>
  <li>
   Cover Letter
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.
 <br/>
 <br/>
 Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.
 <br/>
 <br/>
 For additional questions, please contact michaela-davis-1@uiowa.edu.
 <br/>
 <br/>
 Additional Information
 <br/>
 <br/>
 <ul>
  <li>
   Classification Title: Physician Assistant
  </li>
  <li>
   Appointment Type: SEIU
  </li>
  <li>
   Schedule: Full-time
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compensation
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Pay Level: 11
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Contact Information
 <br/>
 <br/>
 <ul>
  <li>
   Organization: Healthcare
  </li>
  <li>
   Contact Name: Michaela Davis
  </li>
  <li>
   Contact Email: michaela-davis-1@uiowa.edu
  </li>
 </ul>
</div>


Physician Assistant - Weight Management Clinic

The University of Iowa

<p></p><div><div><h3 class="jobSectionHeader"><b>Requisition # 75920</b></h3><h3 class="jobSectionHeader"><b>
Position Basics</b></h3><div><div><div><b><br>
Type of Position</b></div><div> OTHER</div></div><br>
<div><div><b>
Advertising Ends on:</b></div><div> Extended Until Position is Filled</div></div><br>
<div><div><b>
Advertising Started on:</b></div><div> Tuesday, April 28th, 2026</div></div><br>
<div><div><b>
College:</b></div><div> Carver College of Medicine</div></div><br>
<div><div><b>
Department:</b></div><div> Pediatrics</div></div></div><h3 class="jobSectionHeader"><b><br>
Salary</b></h3><div><div><b><br>
Salary:</b></div><div> Commensurate</div></div><h3 class="jobSectionHeader"><b><br>
Position Details</b></h3><div><div><div><b><br>
Full/Part Time Status:</b></div><div> Negotiable</div></div><br>
<div><div><b>
Position Description:</b></div><div><p>
University of Iowa Stead Family Department of Pediatrics seeks a Developmental and Behavioral Pediatrics (DBP) physician. Appointment rank is open and may be to either the tenure track or clinical (non-tenure) track consistent with clinical experience and research interest. Appointment rank to Instructor of Pediatrics (non-tenure or clinical track) may also be considered. The individual selected will join the Division of Developmental and Behavioral Pediatrics to provide patient care, teaching, and consultative services as developmental and behavioral specialist.</p><p><br>
The Division is comprised of five faculty, 3 LIPs, and a DBP Fellow, and is a national leader in research, with NIH-funded grants, including the Hawkeye Intellectual and Developmental Disabilities Research Center (Hawk-IDDRC), as well as industry-sponsored clinical research. In the 2024-25 edition of &ldquo;Best Children&rsquo;s Hospitals,&rdquo; <i>U.S. News &amp; World Report</i> ranked our program as one of the top 50 hospitals for behavioral health. The Division works closely with the University of Iowa Center for Disabilities and Development (CDD), which has been Iowa&rsquo;s University Center for Excellence on Developmental Disabilities (UCEDD) since 1972. The Center for Disabilities and Development integrates a broad array of clinical services in one location, including developmental and behavioral pediatrics, psychology, speech-language pathology, occupational and physical therapy, social work, education, audiology, and nursing, and thus provides an ideal environment for exceptional patient care, education and research. The Center is also the home of Iowa&rsquo;s LEND (Leadership Education in Neurodevelopmental and related Disabilities) program and has provided outstanding interdisciplinary training in neurodevelopmental disabilities for over two decades. This position includes important leadership opportunities, including DBP Fellowship Director and LEND program leadership.</p><p><br>
Fellowship Director applicants would need to meet qualifications as specified by the ACGME (Accreditation Council of Graduate Medical Education). Responsibilities would include 1) designing and overseeing the 3-year curriculum, including clinical experiences, research opportunities, and mentorship; 2) ensuring the fellowship complies with ACGME requirements; 3) managing the recruitment and selection process for fellows, typically through ERAS and the NRMP matching program; and 4) ensuring timely evaluation of fellows&rsquo; clinical, teaching, and research skills.</p><p><br>
The University of Iowa Roy J. and Lucille A. Carver College of Medicine is one of the nation&rsquo;s top medical schools. It is ranked 44th in research by <i>U.S. News &amp; World Report.</i> Stead Family Department of Pediatrics is ranked No. 27 in NIH funding among public pediatric departments nationwide by the Blue Ridge Institute for Medical Research.</p><p><br>
The pediatrics department comprises the medical staff of University of Iowa Health Care Stead Family Children&rsquo;s Hospital, Iowa&rsquo;s only nationally ranked children&rsquo;s hospital and home to the state&rsquo;s only Level 4 NICU and Level 1 Regional Resource Pediatric Trauma Center. The ACGME-accredited pediatric residency program at Stead Family Children&rsquo;s Hospital trains 50 pediatric resident physicians.</p><p><br>
 For its 2024-25 edition of &ldquo;Best Children&rsquo;s Hospitals,&rdquo; <i>U.S. News &amp; World Report</i> ranked Stead Family Children's Hospital in six pediatric specialties: Neonatology, Pediatric and Adolescent Behavioral Health, Pediatric Cancer, Pediatric Diabetes and Endocrinology, Pediatric Nephrology and Pediatric Urology.</p><p><br>
 We are home to the Hawkeye Wave, voted the best college sports tradition by <i>USA Today</i> readers, where 70,000 football fans wave to our patients and providers every game day. You will never feel as much community support as you do at Iowa. Come wave with us!</p><p><br>
For more information contact:</p><p><br>
Lane Strathearn, MBBS, PhD</p><p><br>
Professor of Pediatrics</p><p><br>
Director, Division of Developmental and Behavioral Pediatrics</p><p><br>
Physician Director, Center for Disabilities and Development</p><p><br>
William E. Bell/Gail A. McGuiness Chair for Pediatric Neurodevelopment</p><p><br>
lane-strathearn@uiowa.edu</p><p><br>
Visit us on the web at: https://uihc.org/childrens/</p><p><br>
Successful candidates will be required to self-disclose any misconduct history or pending research misconduct investigation including but not limited to sexual misconduct in prior employment and provide a related release and will be subject to a criminal background and credential check. This applies to clinical, tenure and research positions.</p><p><br>
If your H-1B petition is subject to the September 19, 2025, Presidential Proclamation, please note that the department will not cover the $100,000 payment associated with H-1B sponsorship, either at the time of hire or for international travel purposes. We encourage you to explore alternative pathways for work authorization. Our team is available to help identify options that may be suitable for your situation.</p></div></div><p></p><div><div><b><br>
Education Requirement:</b></div><p>
Must hold an MD/DO degree, or equivalent</p></div><div><div><b><br>
Required Qualifications:</b></div><div><p>
Board certified in Pediatrics, or equivalent</p><p><br>
Board certified in Developmental and Behavioral Pediatrics, or equivalent</p><p><br>
License or eligible for licensure in the State of Iowa</p></div></div><div><div><b><br>
Desirable Qualifications:</b></div><div><p>
Clinical experience in developmental and behavioral pediatrics</p><p><br>
Experience in patient-oriented research</p><p><br>
Teaching competence in pediatrics for medical students and residents</p><p><br>
Evidence of scholarly activity</p><p><br>
Strong oral and written communication and interpersonal skills</p></div></div></div><p></p><h3 class="jobSectionHeader"><b><br>
Online Application Required Documents</b></h3><div><div><div><br>
</div><div> Curriculum Vitae<br>
Letter of Interest</div></div><div><div><p><b><br>
To start the Online Application process for this position, click the &quot;Apply for This Position&quot; button located below the Contact Information.</b></p></div></div></div><h3 class="jobSectionHeader"><b><br>
Contact Information</b></h3><div><div><b><br>
Contact:</b></div><div> Jeanie Cromer <li>jeanie-cromer@uiowa.edu</li><br>
Cmed-Pediatrics<br>
General Hospital<br>
220 Hawkins Drive<br>
GH<br>
Iowa City, IA 52242</div></div></div><div><br>
</div><br>
<p></p><p>The University of Iowa is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment free from discrimination on the basis of race, creed, color, religion, national origin, age, sex, pregnancy (including childbirth and related conditions), disability, genetic information, status as a U.S. veteran, service in the U.S. military, sexual orientation, or associational preferences.</p>
<p>Persons with disabilities may contact University Human Resources/Faculty and Staff Disability Services, (319) 335-2660 or fsds@uiowa.edu, to inquire or discuss accommodation needs.</p>
<p>Prospective employees may review the University Campus Security Policy and the latest annual crime statistics by contacting the Department of Public Safety at 319/335-5022.</p></div>

DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS PHYSICIAN

<div><p>University of Iowa Healthcare, Department of Urology seeks to hire a full-time Clinical Trials Research Associate to design, plan, promote and control clinical trials and coordinate the processing and analysis of trials data. Key areas of responsibility include protocol development/management and study responsibilities; research/clinical activities, subject recruitment and enrollment, data collection and monitoring; regulatory guidelines, documents and submission; and human resources/leadership.</p><p>
Position Responsibilities:</p><div><b>
Protocol Development/Management and Study Responsibilities:</b></div><ul><li><p>
Assist in the design, development, execution, administration and maintenance of protocols and clinical studies.</p></li><li><p>
Oversee CRF development</p></li><li><p>
Review query reports.</p></li><li><p>
Meet with study monitor. Resolve all monitoring issues.</p></li><li><p>
Develop complex research study materials.</p></li><li><p>
Initiate IRB submissions, renewals and communication with constituents.</p></li><li><p>
Liaise with multi-center health care practitioners, agencies and sponsors.</p></li></ul><div></div><p><b><br>
Research/Clinical Activities:</b><b> </b><b>Subject Recruitment and Enrollment:</b></p><ul><li><p>
Responsible for the management and daily activities associated with the assigned projects.</p></li><li><p>
Assist with clinical and data coordination for research activities and set up supplies for study visits and schedule trial-related procedures.</p></li><li><p>
Oversee the recruitment of subjects. Screen, recruit enroll and obtain informed consent for clinical trials.</p></li><li><p>
Oversee the recruitment of subjects by mining databases and EPIC and recruiting subjects from the providers clinics.</p></li><li><p>
Educate study participants on scope of study, potential risks and benefits, possible alternatives and study requirements.</p></li><li><p>
Relay information to principal investigator and verify study participant eligibility.</p></li><li><p>
Collect and document participant study activities.</p></li></ul><p></p><p><b><br>
Data Collection and Monitoring:</b></p><ul><li><p>
Participate in the design, development and testing of clinical research trials data systems.</p></li><li><p>
Validate data, query resolution and make recommendation for resolution.</p></li><li><p>
Revise and implement change in data collection.</p></li><li><p>
Perform all data processing tasks; enter data, verify data, identify problem data, generate queries, etc.</p></li><li><p>
Track study participant data.</p></li></ul><p></p><p><b><br>
Regulatory Guidelines and Documents:</b></p><ul><li><p>
Manage and organize regulatory documentation from sites and regulatory authorities.</p></li><li><p>
Prepare regulatory submissions and start-up activities for new studies.</p></li><li><p>
Perform on-site audits of research and clinical data.</p></li><li><p>
Monitor compliance of regulatory guidelines and proper maintenance of documents.</p></li><li><p>
May recommend corrective action for reportable events.</p></li></ul><div></div><p><b><br>
Human Resources/Leadership:</b></p><ul><li><p>
May provide functional and/or administrative supervision.</p></li><li><p>
Mentor new staff under direction.</p></li></ul><p><b>
 Financial Responsibility:</b></p><ul><li><p>
May develop and manage budget for studies in coordination with Urology Research Administration.</p></li></ul><br>
<div></div>
<div><p><b>Required Qualifications:</b></p><ul><li><p>
A Bachelor&rsquo;s degree or an equivalent combination of education and experience is required.</p></li><li><div>
Minimum 1 year of clinical research or related experience.</div></li><li><p>
Excellent written, verbal and interpersonal communication skills.</p></li><li><div>
Ability to manage complex information with attention to detail and a high level of accuracy.</div></li><li><div>
Proficient in computer software applications.</div></li></ul><p><b>
Desirable Qualifications:</b></p><ul><li><p>
 Prior experience in database software applications (RedCap, BioShare, etc.).</p></li><li><p>
 Knowledge of regulations, guidelines and procedures that apply to human research.</p></li><li><p>
Prior experience with Institutional Review Board (IRB) application materials and processing.</p></li><li><div>
Experience in data collection and entry.</div></li><li><div>
Experience in processing research regulatory documents.</div></li><li><div>
Knowledge of University of Iowa policies, procedures and regulations.</div></li><li><div>
Prior experience in academic medicine, healthcare, or research organization</div></li><li><div>
Knowledge of urology and cancer research.</div></li></ul><div></div><p><b><br>
Application Process:</b></p><p>
In order to be considered for an interview, applicants must upload the following documents and mark them as a &ldquo;Relevant File&rdquo; to the submission:</p><ul><li> Resume</li><li> Cover Letter</li></ul><p>
Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.</p><p></p><p><br>
Successful candidates will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.</p><p></p><p><br>
Hybrid within Iowa: This position may be eligible for a combination of on-campus and remote work within Iowa after the training period is completed. Work arrangement options will be discussed during the hiring process. Per policy, work arrangements will be reviewed annually and must comply with the remote work program and related policies and employee travel policy when working at a remote location.</p><div>
This position is not eligible for University sponsorship for employment authorization.</div><p></p><p><br>
For additional questions, please contact Sandy Moenk at sandy-moenk@uiowa.edu or 319-356-0748.</p></div></div>

Clinical Trials Research Associate - Urology

<div><p>The Holden Comprehensive Cancer Center at the University of Iowa is seeking a Finance Manager with the Clinical Research Services team that will provide oversight for cancer clinical research finance and accounting. Proactively monitors complex accounting functions, ensuring compliance with all university, state, federal, and sponsor requirements. Negotiates budgets and acts as a resource for financial analysts in negotiating budgets with sponsors. Partners with principal investigators, clinical research staff, and administrators to increase understand of research finances and ensure transparent, compliant, and efficient management of oncology clinical research funding. Partners with leadership to support cross-departmental initiatives and organizational efforts to improve financial compliance and operational efficiency.</p><p><b>
This position is eligible for hybrid or remote work within Iowa and will require a work arrangement form to be completed upon the start of your employment. Per policy, work arrangements will be reviewed annually and must comply with the remote work program and related policies and employee travel policy when working at a remote location.</b></p><p>
Duties to include:</p><p>
Financial Operations and Oversight</p><ul><li><p>
Oversees clinical research financial workflow processes, ensuring efficiency, accuracy, and regulatory compliance.</p></li><li><p>
Continuously evaluate existing procedures for recording financial transactions to determine and implement methods to improve efficiency and accuracy.</p></li><li><p>
Acts as primary contact for issues related to industry, consortium, NCI-sponsored, and investigator-initiated budgets and accounts.</p></li><li><p>
Oversees and participates in clinical trial budget negotiations and preparation.</p></li><li><p>
Validates accuracy of monthly transactions, ensuring timely sponsor invoicing, subject reimbursements, and vendor payments.</p></li><li><p>
Participates in cross-functional committees, making recommendations and implementing change as appropriate.</p></li><li><p>
Assists in orientation and education of new staff and faculty regarding the clinical trial financial process and expectations</p></li><li><p>
Oversees the reviews of open trials, ensuring accurate financial reconciliation and implementing corrective actions for billing and compliance issue</p></li></ul><p>
Compliance &amp; Risk Management</p><ul><li><p>
Works closely with the Research Billing Compliance department of Patient Financial Services to identity opportunities to improve communication and workflows related to financial information.</p></li><li><p>
Coordinates Medicare Coverage Analyses with internal staff and external vendors and ensures alignment with the OnCore CTMS system.</p></li><li><p>
Acts as resource for internal and external audit procedures.</p></li><li><p>
Develops and implements internal controls to ensure adherence to university, state, federal, and sponsor guidelines.</p></li><li><p>
Collaborates with compliance offices (e.g., Joint Office for Compliance, Research Billing Compliance) to identify and mitigate risks.</p></li></ul><p>
Team Leadership &amp; Supervision</p><ul><li><p>
Provides administrative supervision of financial analysts, including performance management, workload assessment, and professional development.</p></li><li><p>
Establishes audit and monitoring systems to evaluate staff performance and ensure adherence to financial and compliance standards.</p></li><li><p>
Leads hiring, onboarding, and training of finance staff.</p></li><li><p>
Develops and maintains guidance documents, SOPs, and training resources for finance, regulatory, and clinical research teams.</p></li><li><p>
Designs and implements career ladder frameworks, competencies, and retention strategies in collaboration with HR to support staff growth.</p></li></ul><p>
Reporting &amp; Strategic Support</p><ul><li><p>
Oversees the preparation and analysis of monthly financial reports for HCCC leadership regarding trial revenue and expenditures</p></li><li><p>
Designs and delivers reporting tools to support principal investigators&rsquo; understanding of trial finances.</p></li><li><p>
Prepares specialized financial analyses and recommendations for leadership decision-making.</p></li><li><p>
Identifies emerging financial and compliance risks and advises leadership on process or policy changes.</p></li><li><p>
Provides financial and operational leadership for large-scale initiatives (e.g., billing system modernization, departmental integration efforts).</p></li></ul><p>
Strategic Planning &amp; Workflow Optimization</p><ul><li><p>
Provide strategic leadership in the development, implementation, and continuous improvement of post-award clinical research financial workflows to ensure efficiency, compliance, and alignment with institutional goals.</p></li><li><p>
Serve as a key stakeholder in the planning, decision-making, and cross-functional collaboration for the billing integration between the institution&rsquo;s clinical trials management and electronic medical record systems (e.g. OnCore and Epic) as it relates to clinical research finance, billing, and compliance, ensuring optimized processes and data accuracy.</p></li><li><p>
Identify opportunities to streamline financial operations and drive process improvement.</p></li></ul><p></p><p><b><br>
SUPERVISION RECEIVED:</b></p><p>
 Direct administrative supervision is exercised over all financial analysts in HCCC Clinical Research Services.</p><p>
 Functional supervision for the pre-study finance team is provided by the Regulatory and Compliance Manager for activation of trials.</p><p><b>
SUPERVISION EXERCISED:</b></p><p>
The Finance Manager reports to the Assistant Director for and collaborates extensively with the Medical Director for CPDM and the Associate Director for Clinical Research.</p><p></p><div><p><b><br>
UI Health Care Core Values (WE CARE)</b></p></div><br>
<div><div><p><b><i>
W</i></b><i>elcoming</i></p><p><i><br>
We are welcoming to the community, partners, staff, and patients utilizing the collective strength of our people.</i></p></div><div><p><b><i><br>
E</i></b><i>xcellence</i></p><p><i><br>
We achieve and deliver our personal and collective best in the pursuit of quality and accessible health care, education, and research.</i></p></div><div><p><b><i><br>
C</i></b><i>ollaboration</i></p><p><i><br>
We collaborate with health care systems, providers, and communities across Iowa and the region as well within our UI community. We believe teamwork- guided by compassion- is the best way to work.</i></p></div><div><p><b><i><br>
A</i></b><i>ccountability</i></p><p><i><br>
We behave ethically, act openly and with integrity in all that we do, taking responsibility for our actions.</i></p></div><div><p><b><i><br>
R</i></b><i>espect</i><i><br>
</i></p><p><i>We create an environment where every individual feels safe, valued, and respected, supporting the well-being and success of all members of our community.</i></p></div><div><p><b><i><br>
E</i></b><i>mpowerment</i></p><p><i><br>
We commit to fair access to research, health care, and education for our community and opportunities for personal and professional growth for our staff and learners.</i></p></div><br>
</div><p>
University of Iowa Health Care&mdash;recognized as one of the best hospitals in the United States&mdash;is Iowa's only comprehensive academic medical center and a regional referral center. Each day more than 12,000 employees, students, and volunteers work together to provide safe, quality health care and excellent service for our patients. Simply stated, our mission is: Changing Medicine. Changing Lives.&reg;</p><p>
Holden Comprehensive Cancer Center is Iowa&rsquo;s only NCI-designated comprehensive cancer center. The NCI designation recognized our cancer center, and its research scientist, physicians, and other health care professionals, for their roles in advancing cancer research that impacts on our ability to prevent, detect and treat our patients with cancer. Not just a floor, or a building, or even confined to a single college. Holden Comprehensive Cancer Center coordinates all cancer-related research, education, and patient care by faculty from 41 departments and six colleges, as well as UI Health Care and UI Children&rsquo;s Hospital.</p><p><b>
Percent of Time:</b> 100%</p><p><b>
Work Schedule: </b>Monday &ndash; Friday, Hours generally worked between 7:00am-5pm</p><p><b>
Pay Grade: </b>5B</p><p>
https://hr.uiowa.edu/pay/guide-pay-plans</p><p><b>
Benefits Highlights</b></p><ul><li><p>
Regular salaried position located in Iowa City, IA</p></li><li><p>
Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans</p></li><li><p>
For more information about Why Iowa?, click here</p></li></ul>
<div><div><b>REQUIRED QUALIFICATIONS</b></div><ul><li><div>
 Master&rsquo;s degree in a Business, Accounting or related field, or an equivalent combination of education and experience.</div></li><li><div>
 3 -5 years of experience in accounting, finance, and/or project management</div></li><div></div><li><div><br>
 1-3 years of supervisory experience that includes financial management as well as performance management and staff development</div></li><li><div>
 Experience with financial contracts, sponsor invoicing, and revenue reconciliation</div></li><li><div>
 Experience with billing compliance requirements and close out procedures</div></li><li><div>
 Excellent written, verbal, and interpersonal communication skills</div></li><li><div>
 Strong attention to detail and proven ability to manage complex workflows</div></li><li><div>
 Demonstrated proficiency in computer software applications including Microsoft products and various databases.</div></li></ul><div></div><div><b><br>
HIGHLY DESIRED QUALIFICATIONS</b></div><ul><li><div>
 Demonstrated experience in clinical trial budget development and negotiation including investigator initiated and industry sponsored trials.</div></li><li><div>
 Demonstrated expertise in complex budget development</div></li><li><div>
 Demonstrated knowledge of Medicare Coverage Analysis and its application to clinical trial</div></li></ul><div></div><p><b><br>
DESIRED QUALIFICATIONS</b></p><ul><li><p>
Experience with insurance and healthcare billing processes</p></li><li><p>
Familiarity with Advarra OnCore CTMS, including financial modules</p></li><li><p>
Knowledge of medical terminology and clinical trial operations</p></li><li><p>
Knowledge of University of Iowa accounting policies, procedures, and systems</p></li></ul><p></p><p><b><br>
Application Process:</b> In order to be considered, applicants must upload <b>a resume and cover letter</b>(under submission relevant materials) that clearly address how they meet the listed required and desired qualifications of this position.</p><p>
Job openings are posted for a minimum of <b>7 </b>calendar days.</p><p>
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification.</p><p>
References: Five professional references will be requested and required at a later step in the recruitment process</p><p>
With additional questions, please reach out to Sarah Waldschmidt at sarah-waldschmidt@uiowa.edu</p></div></div>

Clinical Research Finance Manager - Remote - Cancer Center

<div><p>The University of Iowa Health Care is seeking a patient centered <b>Care Team Coordinator (CTC) 100% (40 hours a week) </b>to work in our <b>Dermatology Bettendorf Clinic</b>. This position supports our team-based care where you&rsquo;ll spend more time with patients and expand your physician-support and administrative duties, increases the efficiency and productivity of the physician and anticipates future needs to facilitate the flow of the clinic. Accurately documents events and decision-making in a manner that results in appropriate medical charting. Our team specialize in the care of everyone in the family, in every generation, from birth, for life.</p><p>
Our <b>Care Team Coordinator </b>(Medical Assistant)<b> </b>provide full medical and surgical services, from general dermatology care to specialty services, to patients with skin diseases. We use the latest techniques to care for a range of conditions affecting the skin. We also work closely with you to take precautions against skin cancer, infections, dry skin and the aging effects of sun exposure. Our services include treatment of cosmetic skin problems such as age spots and birthmarks and the removal of unwanted hair and tattoos. We offer chemical peels, Botox injections and dermal fillers. We also offer general dermatology services, and we offer quick scheduling for appointments.</p><p>
Our <b>Care Team Coordinator's </b>(Medical Assistant)<b> </b>accompany the physicians or medical providers into the examination rooms in order to transcribe the clinician&rsquo;s and care team&rsquo;s encounter with the patients in real time. They accurately and thoroughly document the encounter with our patients as it is being performed by the providers, which may include documentation in the following sections: problem list, history of present illness, review of systems, physical exam, assessment and plan, procedures and treatments performed by team, patient education, orders, medications, referrals, explanations of risks and benefits, and instructions for self-care and follow-up.</p><p><b>
This position will mainly support our Dermatology Clinics but could float to other patient specialties/clinic locations including but not limited to: Pediatrics and/or Specialty/Outreach Clinics.</b></p><p>
This position comes with the University of Iowa's generous, <b><i>full benefit package</i></b><b> </b>including double-match retirement, paid vacation, and sick leave, and much more! This position also includes <b><i>FREE </i></b><b>on-site parking as well!</b></p><p><b>
Summary:</b></p><p>
Under direct supervision of LIP (licensed independent practitioner), RN (registered nurse), NM/ANM (nurse manager/assistant nurse manager) or other licensed designee, functions as a member of the patient care team. Performs technical, patient care and related clerical functions in the clinic setting by coordinating all elements of the patient visit. Enters information into the electronic medical record at the direction of the physician or licensed independent practitioner. Increases the efficiency and productivity of the physician and anticipates future needs to facilitate the flow of the clinic. Accurately documents events and decision-making in a manner that results in appropriate medical charting. Performs technical and patient care responsibilities as directed by physician or licensed independent practitioner.</p><p>
University of Iowa Health Care&mdash;recognized as one of the best hospitals in the United States&mdash;is Iowa's only comprehensive academic medical center and a regional referral center. Each day more than 12,000 employees, students, and volunteers work together to provide safe, quality health care and excellent service for our patients. Simply stated, our mission is: Changing Medicine. Changing Lives.&reg;</p><p><b>
Duties to include:</b></p><ul><li>
Performs patient care responsibilities of a Medical Assistant or other certified health care provider including, but not limited to, assisting with physical examinations, administering routine medications, performing routine laboratory tests, and operating and maintaining specialized medical equipment.</li><li>
Responsible for the daily flow of the Care Team and facilitates daily team huddles. The Care Team Coordinator understands clinic flow to maximize clinic usage to meet patient needs.</li><li>
Follows enhanced and standard patient rooming protocols. Prepares the clinic note for the patient visit by manually bringing in provider-built Electronic Medical Record (EMR) documentation tools for the following sections: history of present illness, review of system, physical exam, assessment and plan. Ensures health maintenance section (including quality reporting measures) and immunizations are up to date.</li><li>
Populates patient-reported information into provider-built EMR documentation tools for the specific disease states and preventative visits.</li><li>
Reviews EMR for patient care gaps, addresses and updates missing data.</li><li>
Communicates a summary of the patient-reported information to the provider prior to entry of the room or within the room with the patient present.</li><li>
Accompanies the physician or medical provider into the examination room in order to transcribe the clinician&rsquo;s and care team&rsquo;s encounter with the patient in real time.</li><li>
Accurately and thoroughly documents the encounter with the patient as it is being performed by the provider, which may include documentation in the following sections: problem list, history of present illness, review of systems, physical exam, assessment and plan, procedures and treatments performed by team, patient education, orders, medications, referrals, explanations of risks and benefits, and instructions for self-care and follow-up.</li><li>
Appropriately documents results of laboratory and radiographic studies as dictated by the clinician. Organizes all patient test results and transcribes the results of the encounter into the patient&rsquo;s medical record.</li><li>
Responsible for the input of orders for provider signature or signing orders (per protocol) as directed by the provider. This may include referral orders, medication refill orders, imaging orders, or lab orders.</li><li>
Identifies the portions of the encounter that were scribed on behalf of the provider using the scribe signature per policy.</li><li>
Schedules future appointments, referrals, procedures, and diagnostics as appropriate.</li><li>
Provides patient instruction using pre-approved patient education materials specific to the chief complaint or for the health promotion of observed behaviors known to contribute to poor health, as directed by the provider.</li><li>
Prints after visit summary and completes discharge of patient from exam room.</li><li>
Provides age-appropriate care/service as applicable to role.</li><li>
Assures reliable, predictable outcomes and no needless waits.</li><li>
Acts as patient advocate to ensure all concerns are met and engages extended care team members as appropriate.</li><li>
Participates in and supports quality improvement activities in the clinic and implementing evidenced based practice (EBP) research best practices.</li></ul><p><b>
WE CARE Core Values:</b></p><ul><li><b>
Welcoming</b> - We strive for an environment where everyone has a voice that is heard, that promotes the dignity of our patients, trainees, and employees, and allows all to thrive in their health, work, research, and education.</li><li><b>
Excellence</b> - We aim to achieve and deliver our personal and collective best in the pursuit of quality and accessible healthcare, education, and research.</li><li><b>
Collaboration</b> - We encourage collaboration with healthcare systems, providers, and communities across Iowa and the region, as well as within our UI community. We believe teamwork - guided by compassion - is the best way to work.</li><li><b>
Accountability</b> - We behave ethically, act with fairness and integrity, take responsibility for our own actions, and respond when errors in behavior or judgment occur.</li><li><b>
Respect</b> - We create an environment where every individual feels safe, valued, and respected, supporting the well-being and success of all members of our community.</li><li><b>
Empowerment</b> - We commit to fair access to research, health care, and education for our community and opportunities for personal and professional growth for our staff and learners.</li></ul><div><b>
Benefits Highlights:</b><br>
<ul><li>Regular salaried position located in Bettendorf, IA (and surrounding clinics based on clinical need/hours)</li><li>The University of Iowa offers a generous benefits package, including paid vacation as well as paid sick leave. Complete information regarding the full benefits package may be viewed at: https://hr.uiowa.edu/benefits</li></ul></div><p><b>
Percent of Time: </b>100% (40 hours per week)</p><p><b>
Schedule:</b> Variable hours accomplished between Monday - Friday from 7:30 AM &ndash; 5:30 PM; no weekends, no on-call and no holidays.</p><p><b>
Location: </b>Bettendorf, IA (and surrounding clinics based on clinical need/hours)</p><p><b>
Pay Grade: </b>10 https://hr.uiowa.edu/pay/merit-plan</p><p><b>
Salary:</b> $42,699.60 to $63,496.08 (<b><i>based on years of experience</i></b>)</p>
<div><p><b>Minimum Eligibility Requirements</b></p><ul><li>
Two years of work experience as a Medical Assistant or other health care provider involving direct patient care, <b>and</b></li><li>
Certification <b>OR </b>registration as a Medical Assistant <b>OR </b>completion of a recognized one year Medical Assistant Program, <b>OR </b>Completion of a health care profession program with a curriculum incorporating technical patient care elements including but not limited to: pathophysiology, medical terminology, basic pharmacology and medication administration including dose calculation and psychology.</li></ul><p><b>
Special Qualifications/Licenses:</b></p><ul><li>
Driver's License and ability to meet UI Fleet Safety Standards.</li><li>
Availability to provide support to other clinical locations as needed.</li></ul><p><b>
Highly Desirable Qualifications</b></p><ul><li>
The ability to adapt quickly to different clinical environments and patient populations is highly desired.</li></ul><p><b>
Desirable Qualifications</b></p><ul><li>
Minimum 6 months ambulatory experience.</li><li>
Previous EPIC experience.</li><li>
Demonstrated experience fostering a welcoming and respectful work/academic environment.</li></ul><p>
Staff may be required to receive a passing score on work samples to be considered for this position.</p><p>
In order to be considered, <b><i>applicants must upload resume</i></b> (under submission relevant materials) that clearly address how they meet the listed required and desired qualifications of this position.</p><p>
Job openings are posted for a minimum of 10 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. For questions or additional information, please contact: Jiberle-Mustefa@uiowa.edu</p><div>
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check. This position is not eligible for University sponsorship for employment authorization.</div></div></div>

Care Team Coordinator/CMA - UI Health Care Bettendorf Dermatology Clinic 100%

<div><p>The Clinical Trial &amp; Data Management Research Associate role in Emergency Medicine (EM) will be an integral member of the research team. This position will provide support for Emergency Medicine working alongside the ICTS team performing activities which are vitally important to grow and foster innovation through research support endeavors. This position will apply clinical skills to administer, deliver, and evaluate research protocols.</p><p><b>
Research/Clinical Activities, Subject Recruitment and Enrollment</b></p><ul><li><div>
Screen participant for study eligibility.</div></li><li><div>
Educate participant on scope of study, potential risks and benefits, possible alternatives, and study requirements for participant.</div></li><li><div>
Communicate with principal investigator and verify participant eligibility.</div></li><li><div>
Administer study treatments and identify adverse reactions.</div></li><li><div>
Recruit, enroll and obtain informed consent for clinical research activities. Oversee the recruitment of participants and scheduling of trial-related procedures.</div></li><li><div>
Prepare study recruitment materials. Develop complex study recruitment materials.</div></li></ul><p><b>
Protocol Development/Management and Study Responsibilities</b></p><ul><li><div>
Collaborate with Principal Investigator and the study team in the development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures.</div></li><li><div>
Assess participants for problems related to protocol. Oversee CRF development, database development and maintenance.</div></li><li><div>
Review query reports. Resolve all monitoring visit issues.</div></li><li><div>
Perform and monitor randomizations.</div></li><li><div>
Develop complex study materials used in conduction of study.</div></li><li><div>
Communicate with local health care practitioners, agencies, and sponsors as needed.</div></li></ul><p><b>
Data Collection and Monitoring</b></p><ul><li><div>
Participate in the design, development, and testing of clinical research trial data systems.</div></li><li><div>
Maintain communication between health care clinical information systems and research data systems.</div></li><li><div>
Collect and validate data. Make recommendations for query resolution.</div></li><li><div>
Assist with identification of data problems and implement change as needed.</div></li></ul><p><b>
Regulatory Guidelines and Documents</b></p><ul><li><div>
Manage and organize regulatory documentation.</div></li><li><div>
Prepare and submit regulatory documents.</div></li><li><div>
Assist sponsor with on-site audits of research and clinical data.</div></li><li><div>
Monitor and maintain compliance of regulatory guidelines and documents.</div></li><li><div>
Prepare and present Institutional Review Boards or other submissions and required regulatory documents.</div></li><li><div>
Carry out corrective action plan for reportable events.</div></li></ul><p><b>
Financial Responsibility</b></p><ul><li><div>
Assist in the development and administer study budgets.</div></li><li><div>
Participate in preparation of grant applications for extramural funding.</div></li><li><div>
Oversee internal pilot funding program application process.</div></li><li><div>
Assist with tracking and reconciling grant budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded.</div></li></ul>
<div><p><b>Education Requirements: </b>A Bachelor&rsquo;s degree in a Health Science field or an equivalent combination of education and research experience.<b>:</b></p><ul><li>
A Bachelor&rsquo;s degree in a Health Science field or an equivalent combination of education and research experience.</li></ul><p><b>
Experience Requirements:</b></p><ul><li><div>
A minimum of one year experience designing, developing, and implementing recruitment program materials.</div></li><li><div>
Working knowledge of Good Clinical Practice (GCP) in research.</div></li><li><div>
Excellent written and verbal communication skills.</div></li><li><div>
Ability to work nights and weekends.</div></li><li><div>
Must be proficient in computer software applications (MS Word, Excel, PowerPoint, and Outlook).</div></li></ul><p><b>
Desired Qualifications:</b></p><div><ul><li><div>
Experience with REDCap, Epic and ACCESS.</div></li></ul></div><div><ul><li><div>
Previous experience in data collection and entry.</div></li></ul></div><div><ul><li><div>
Experience in processing research regulatory documents and ethics preparation.</div></li></ul></div><div><ul><li><div>
Excellent time management skills and ability to perform detail oriented work.</div></li></ul></div><div><ul><li><div>
1-3 years of clinical research experience.</div></li></ul></div><div><ul><li><div>
Experience developing and working with research budgets/billing.</div></li></ul></div><div><ul><li><div>
A current, valid Registered Nurse license or Respiratory Therapist license.</div></li></ul></div><div><ul><li><div>
Database management experience including entering, tracking and maintaining data and troubleshooting</div></li></ul></div><p>
Application Process: In order to be considered, applications <b>must </b>upload a resume. Job openings are posted for a minimum of 7 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. For questions or additional information, please contact Katie McVay at katie-mcvay@uiowa.edu. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.</p></div></div>

100% Clinical Trial & Data Management Research Associate - Emergency Medicine

Explore 62+ Clinical trials research assistant or associate pediatrics endocrine diabetes in Iowa City this May. Find roles across top companies and apply now to boost your career.