clinical research coordinator i

University of Alabama, Birmingham

<div></div><div><div><div><div><div><b>Description</b><div></div><p>
The University of Alabama at Birmingham (UAB), Med - Hematology &amp; Oncology, is seeking a Clinical Research Coordinator I to recruit patients for studies, conduct follow-up interviews with patients and providers, and perform quality analysis.</p><p><b>
General Responsibilities</b></p><ul><li><p>
To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.</p></li><li><p>
To support screening and participant eligibility determination, working with more senior team members to ensure compliance.</p></li><li><p>
To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).</p></li><li><p>
To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.</p></li></ul><p><b>
Key Duties &amp; Responsibilities</b></p><ul><li><p>
Collects and documents data for clinical research programs. Recruits and performs followup with research participants as protocols outline. Schedules visits according to research protocols.</p></li><li><p>
Assists in coordination of lab and fieldwork. Coordinates appointments for additional procedures as necessary. Prepares for and participates in study monitoring visits. Assists with correcting findings. Participates in study meetings and conference calls.</p></li><li><p>
Assists with the completion of Case Report Forms (CRF) according to protocol.</p></li><li><p>
May assist with development of protocols and standard operating procedures (SOPs) for data quality assurance.</p></li><li><p>
Performs administrative duties in support of research conduction as needed.</p></li><li><p>
Prepares source documentation for review with investigators. May perform a variety of medical procedures under supervision.</p></li><li><p>
May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.</p></li><li><p>
May use Electronic Data Capture (EDC) systems necessary for operations under supervision.</p></li><li><p>
Performs other duties as assigned.</p></li></ul><p><b>
Annual Salary Range</b>: $43,890 - $71,320</p><div><br>
</div></div><div><b>
Qualifications</b><div></div><p>
High School diploma or GED required.</p><p><b>
Preferences</b></p><ul><li><p>
The ideal candidate will have a background in analyzing data.</p></li></ul><p><br>
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.</p><div><br>
</div></div><div><b>
Primary Location</b><b>:</b> University</div><div><b>
Job Category</b><b>:</b> Clinical Research</div><div><b>
Organization</b><b>:</b> 311402200 Med - Hematology &amp; Oncology</div><div><b>
Employee Status</b><b>:</b> Regular</div><div><b>
Shift</b><b>:</b> Day/1st Shift</div><div><b>
Work Arrangement (final schedule to be determined by the department/hiring manager)</b><b>:</b> Remote/Hybrid Eligible</div></div></div></div></div><div></div>

CLINICAL RESEARCH COORDINATOR I

Children's Hospital Los Angeles

<div>Location/Org Data : Introduction:
<div>
Join a team that's shaping the future of pediatric care. Children&rsquo;s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services. Here, world-class experts in medicine, research, and education work together to deliver family-centered care to more than 155,000 patients each year. At CHLA, your work will help build brighter tomorrows for the children and families we serve.</div>
Overview:
<div><b>
Schedule:</b> Monday-Friday, Day Shift</div><div></div><div><b><br>
Purpose Statement/Position Summary:</b> The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects.<br>
<br>
<b>Minimum Qualifications/Work Experience:</b> 1+ years of experience in clinical trial coordination or computerized databases. 1 year of clinical research (study coordination, data management) or related experience preferred. Contracts, budgets, invoicing, and regulatory experience preferred.<br>
<br>
<b>Education/Licensure/Certifications:</b> High School Diploma, GED, or equivalent required. Bachelor's degree in related scientific field preferred. Certified clinical research associate/coordinator preferred.</div>
Pay Scale Information: CHLA values the contribution each Team Member brings to our organization. Final determination of a successful candidate&rsquo;s starting pay will vary based on a number of factors, including, but not limited to, education and experience within the job or the industry. The pay scale listed for this position is generally for candidates who meet the specified qualifications and requirements listed on this specific job description. Additional pay may be determined for those candidates who exceed these specified qualifications and requirements. We provide a competitive compensation package that recognizes your experience, credentials, and education alongside a robust benefits program to meet your needs. Posting Range: $61,152.00-$100,464.00 Location/Org Data : Closing:
<div>
CHLA is a leader in pediatric and adolescent health, in our community, across the nation, and around the world . As a premier Magnet&reg;-recognized teaching hospital, CHLA offers an environment rooted in learning, collaboration, and compassionate care. . We are home to groundbreaking research, clinical innovation, and a culture that supports personal and professional growth.</div><div>
Since 1932, CHLA has been affiliated with the Keck School of Medicine of the University of Southern California. Through this partnership and our own enduring mission, we remain committed to creating hope and building healthier futures.</div></div>

Clinical Research Coordinator I

ObjectiveHealth

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 <strong>
  Clinical Research Coordinator I
  <br/>
  <br/>
 </strong>
 Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.
 <br/>
 <br/>
 <strong>
  Who We Are
  <br/>
  <br/>
 </strong>
 ObjectiveHealth is a clinical research company that uses proprietary technology to:
 <br/>
 <br/>
 <ul>
  <li>
   Increase patient access to research trials within our communities,
  </li>
  <li>
   Provide physicians with enhanced care options for current patients, and
  </li>
  <li>
   Deliver superior clinical research enrollment metrics to Pharma sponsors
   <br/>
   <br/>
  </li>
 </ul>
 All with the goal of
 <em>
  Improving Patient Outcomes at the Point of Care
 </em>
 . We want you to join us in doing just that.
 <br/>
 <br/>
 <strong>
  Who You Are
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   A lover of patient interaction and skilled at providing patient care
  </li>
  <li>
   A team player with a bias for action and an attitude that takes personal responsibility
  </li>
  <li>
   Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
  </li>
  <li>
   Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
  </li>
  <li>
   Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
  </li>
  <li>
   An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
  </li>
  <li>
   A strong advocate for Company values, mission, and initiatives
  </li>
  <li>
   Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
  </li>
  <li>
   Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What Success Looks Like For This Role
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Taking ownership of assigned studies and patients
  </li>
  <li>
   Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
  </li>
  <li>
   Showing up on time, every time
  </li>
  <li>
   Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
  </li>
  <li>
   Learning and using the technologies we provide to increase efficiency in your day-to-day activities
  </li>
  <li>
   Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer
  <br/>
  <br/>
 </strong>
 Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.
</div>


Cedars-Sinai Medical Center

<p></p><div><div><div><div><p><b>Job ID</b> 16507</p>
<p><b>Location</b> California, United States
</p><p><b>Job Category</b> Academic / Research
</p><p><b>Date posted</b> 04/28/2026</p></div></div><p></p><div><br>
<div></div>
</div></div><div><h2 class="jobSectionHeader"><b>Job Description</b></h2><p><b>
Come join the Kidney Transplant Team!</b></p><p>
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).<br>
<br>
<b>Principal Responsibilities:</b><br>
Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.</p><p>
Schedules patients for research visits and procedures.</p><p>
In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.</p><p>
Maintains accurate source documents related to all research procedures.</p><p>
Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.</p><p>
Schedules and participates in monitoring visits, aid in site initiation visits (SIVs), perform close-out visits (COVs), and auditing activities.</p><p>
Communicate with sponsors regarding exceptions and protocol clarifications.</p><p>
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.</p><p>
Notifies direct supervisor about concerns regarding data quality and study conduct.</p><p>
Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.</p><p>
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.</p><p>
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.</p><p>
Maintains research practices using Good Clinical Practice (GCP) guidelines.</p><p>
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.</p><p>
Participates in required training and education programs</p><h2 class="jobSectionHeader"><b>
Qualifications</b></h2><p><b>
Education:</b><br>
High School Diploma/GED, required</p><p>
Bachelor's Degree, Science, Sociology or related degree, preferred<br>
<br>
<b>Work Experience:</b></p><p>
1 year Clinical research related experience required<br>
<br>
<b>Licenses and Certifications:</b></p><p>
Certification In Clinical Research SOCRA or ACRP certification Upon Hire preferred</p>
</div><div><div><div><b>Req ID</b> 16507</div>
</div><div><div><b>Working Title</b> Clinical Research Coordinator I - Kidney Transplant</div>
</div><div><div><b>Department</b> Research - Hepatology</div>
</div><div><div><b>Business Entity</b> Cedars-Sinai Medical Center</div>
</div><div><div><b>Job Category</b> Academic / Research</div>
</div><div><div><b>Job Specialty</b> Research Studies/ Clin Trial</div>
</div><p></p><div><div><b>Overtime Status</b> NONEXEMPT</div>
</div><div><div><b>Primary Shift</b> Day</div>
</div><div><div><b>Shift Duration</b> 8 hour</div>
</div><div><div><b>Base Pay</b> $24.00 - $39.76</div></div></div></div><p></p>
<br><div><div><h3 class="jobSectionHeader"><b>Diversity and Inclusion at Cedars-Sinai</b></h3>
<div>
We are caretakers and innovators committed to the pursuit of equitable healthcare. But health equity is not possible without representation. Our commitment to diversity goes beyond demographics or checking boxes. Our people must reflect the diverse identities, experiences and geographies of the communities and patients we serve &ndash; because that&rsquo;s what our patients, colleagues and communities deserve <b>Quality Care and Research&mdash;For All, By All</b>.</div>
</div><div><h3 class="jobSectionHeader"><b>Cedars-Sinai is an Equal Employment Opportunity employer.</b></h3>
<p>
Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at <b>Applicant_Accommodation@cshs.org</b> and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.</p>
<p>
Cedars-Sinai will consider for employment qualified applicants with criminal histories, in accordance with the Los Angeles Fair Chance Initiative for Hiring.</p>
<p>
At Cedars-Sinai, we are dedicated to the safety, health and wellbeing of our patients and employees. This includes protecting our patients from communicable diseases, such as influenza (flu). For this reason, we require that all new employees receive a flu vaccine based on the seasonal availability of flu vaccine (typically during September through April each year) as a condition of employment, and annually thereafter as a condition of continued employment, subject to medical exemption or religious accommodation. For the same reason, you may also be required to receive other vaccines as a condition of employment. Cedars-Sinai reserves the right to make modifications to its required list of vaccines as required by law and/or policy.</p></div></div><div></div>

Benaroya Research Institute

<div>Overview:
<div>
The Benaroya Research Institute (BRI) and Virginia Mason Medical Center (VMMC) seek a Clinical Research Coordinator (CRC) to join our Digestive Health Clinical Research team. The Center for Digestive Health at Virginia Mason is internationally known for bringing experts together to optimize care through innovations in research, education, and a multidisciplinary approach to treatment of digestive and liver diseases. Virginia Mason Franciscan Health was named by Healthgrades&reg; as America&rsquo;s 100 Best Hospitals for Gastrointestinal Care.</div><div></div><div><br>
The Clinical Research Coordinator I will oversee daily clinical trial operations, ensuring protocol compliance, coordinating patient visits, managing data, and facilitating communication among investigators, participants, and regulatory bodies. The ideal candidate will have a strong clinical research background, excellent organizational skills, and the ability to communicate complex information effectively. This role offers the opportunity to contribute to groundbreaking research aimed at improving treatments for digestive diseases alongside a team of dedicated experts.</div><div></div><div><br>
Hybrid work may be allowed occasionally depending on workload, research patient schedule, and job performance. The work schedule may vary - it is typically Monday through Friday, from 8:00 AM to 4:30 PM, with a 30-minute lunch break.</div>
Responsibilities:
<ul><li>Facilitate clinical research, including collaboration with affiliate or partnering research sites and conducting BRI-based studies</li><li>
Prepare for new studies, including regulatory document filing and study monitor visit preparation</li><li>
Screen and recruit study subjects, obtain informed consent, and document subject history</li><li>
Review adverse events, concomitant medications, and ensure protocol compliance and subject safety</li><li>
Handle test articles (TA), complete case report forms, and maintain source documents</li><li>
Manage proper standard or research billing and ensure site quality</li><li>
Coordinate subject care, including appointment scheduling, record reviews, treatment coordination, and health assessments</li><li>
Collect vital signs, perform telephone triage/screening, and assist with subject arrivals</li><li>
Conduct phlebotomy, specimen processing using universal precautions, and other procedures as appropriate</li><li>
Participate in process improvement activities and develop corrective and preventive action plans</li></ul>
Qualifications:
<ul><li>Minimum of one year full-time related experience required</li><li>
Must maintain subject and document confidentiality at all times</li><li>
Understand and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, IRB, and institutional policies and procedures</li><li>
Requires good medical knowledge, including medical terminology and basic subject care</li><li>
May require phlebotomy and vital sign collection skills, as well as the ability to operate centrifuges and EKG machines</li><li>
Preferred: Higher education or vocational training specializing in healthcare</li><li>
May require healthcare licensure or other specialized training</li></ul>
Compensation:
<div>
 $25.66 to $37.21 hourly</div>
Benefits:
<ul><li>Medical, dental, vision insurance</li><li>
Flexible spending accounts: health care, dependent care, commuter</li><li>
Short and long-term disability</li><li>
Life and AD&amp;D insurance</li><li>
403(b) retirement plan with matching funds after one year of employment</li><li>
PTO: 13 holidays, three weeks of vacation and two weeks of sick leave per year</li><li>
Employee assistance program</li><li>
Educational assistance program</li><li>
Subsidized ORCA pass</li><li>
Wellness benefits</li><li>
Voluntary benefits</li></ul>
About Us:
<div>
The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to patients, giving them access to clinical trials for over 100 different conditions including cancer, digestive disease, cardiology, and neuroscience. The Clinical Research Program at BRI oversees all clinical research at Virginia Mason Medical Center, combining the expertise of a world-renowned research institute with remarkable healthcare to support studies that contribute to improving the diagnosis, treatment, and prevention of a variety of diseases.</div><div></div><div><br>
BRI is an independent, nonprofit research institute affiliated with Virginia Mason Franciscan Health and based in Seattle. Our culture is based on the values of collaboration, respect, innovation, and inquiry; team members work together to support patients and clinicians with the goal of better outcomes for all.</div><div></div><div><br>
At BRI, each role is valued and an important contributor to our vision and mission. BRI is committed to a safe, caring and diverse workplace; as well as to taking action to further our commitments to foster inclusion, equity and belonging so employees feel comfortable bringing their full selves to work. Consider making a difference by joining our team. Because together, we are <b>powering possibility.</b><br>
<br>
To learn more, visit benaroyaresearch.org and connect with us on Facebook, Instagram, Threads, LinkedIn, Bluesky and YouTube.<br>
<br>
<b>Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. If you need an accommodation or assistance completing the online application, please contact Human Resources at 206-342-6547 or email </b><b>jobs@benaroyaresearch.org.</b> <b>This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.</b></div></div>

Roswell Park Comprehensive Cancer Center

<div><h2 class="jobSectionHeader"><b>Title:
</b></h2>Clinical Research Coordinator I<p><b>
Job Type:</b></p>
Regular<h2 class="jobSectionHeader"><b>
Company:</b></h2>
Health Research, Inc. (HRI) Roswell Park Division<h2 class="jobSectionHeader"><b>
Department:
</b></h2>Clinical Trials Office<h2 class="jobSectionHeader"><b>
Time Type:
</b></h2>Full time<h2 class="jobSectionHeader"><b>
Weekly Hours:
</b></h2>40<p><b>
FTE:</b></p>
1<h2 class="jobSectionHeader"><b>
Shift:
</b></h2>First Shift (United States of America)<p></p><h2 class="jobSectionHeader"><b>
Summary:
</b></h2>Manages and coordinates the care of patients participating in a clinical research study with guidance from preceptor, educator and/or administrator; educates patients, families and staff regarding study compliance; collects a complete and accurate study data set and facilitates accrual to clinical research studies. The salary range for this position is $77,264 - $95,529 annually which includes a geographic differential and comprehensive benefits package. The listed pay range reflects the range of potential compensation for this role. The actual offer may vary based on qualifications, skills, and experience.<p></p><h2 class="jobSectionHeader"><b>
Qualifications:</b></h2>
Required Education and Experience<br>
<br>
Certification Requirement<br>
1. Current certification by the Association of Clinical Research Professionals (ACRP); or<br>
2. Current certification by the Society of Clinical Research Associates (SOCRA); or<br>
3. Other comparable research-related certifications recognized by Roswell Park Comprehensive Cancer Center as appropriate for this title.<br>
<br>
Education and Experience<br>
1. Bachelor&rsquo;s degree and the equivalent of one (1) year of full-time clinical research, healthcare or other related experience; or<br>
2. Associate&rsquo;s degree and the equivalent of two (2) years of full-time clinical research, healthcare or other related experience, including successful completion of a Clinical Research Coordinator traineeship at Roswell Park Comprehensive Cancer Center (Roswell Park); or<br>
3. Associate&rsquo;s degree and the equivalent of three (3) years of full-time clinical research, healthcare or other related experience; or<br>
4. High School Diploma or High School Equivalency Diploma and four (4) years of full-time clinical research, healthcare or other related experience, including successful completion of a Clinical Research Coordinator traineeship at Roswell Park Comprehensive Cancer Center (Roswell Park); or<br>
5. High School Diploma or High School Equivalency Diploma and five (5) years of full-time clinical research, healthcare or other related experience.<br>
<br>
NOTE:<br>
1. Incumbents must obtain and maintain certification through the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA) or from other comparable research-related certifications recognized by Roswell Park Comprehensive Cancer Center as appropriate for this title within five (5) years of appointment as a condition of continued employment.<br>
2. Degrees must be conferred by an accredited school, college, or university, or by an institution recognized by Roswell Park Comprehensive Cancer Center and/or Health Research Incorporated as adhering to acceptable educational standards.<p></p><p>
Preferred Qualificaitons:</p><p></p><p>
The preferred candidate will have:</p><p></p><p>
Previous Clinical Research Experience @Academic Medical Center</p><p>
Previous Clinical Oncology experience</p><p>
Certification by either ACRP or SoCRA</p><p>
Bachelor's degree in Life Sciences or Medical Field</p><p>
Experience with FDA regulations and GCP/ICH guidance</p><p>
Citi Course training completed</p><p>
Previous experience with Serious Adverse Event and UP reporting</p><p></p><p><b>
Equal Employment Opportunity Statement</b></p><p>
Roswell Park Cancer Institute Corporation (RPCIC) and Health Research Inc. (HRI) Roswell Park Division believe that all persons are entitled to equal employment opportunities, and we do not discriminate against our employees, applicants or job seekers because of their race, color, religion, sex, sexual orientation, gender identity or expression, national origin, creed, age, disability, pregnancy-related condition, military or veteran status, marital or familial status, domestic violence victim status, citizenship status, genetic information, individual&rsquo;s relationship or association with a member of a protected category or any other protected group status as defined by law.</p><p></p><p>
Affirmative Action/Equal Opportunity Employer/Qualified Individuals with Disabilities/Qualified Protected Veterans</p><p></p><p><b>
Reasonable Accommodation Request</b></p><p>
RPCIC and HRI are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email HR-PayAndBenefits@RoswellPark.org and let us know the nature of your request and your contact information.</p><p></p><p><b>
Our Core Values</b></p><p>
RPCIC and HRI are committed to providing an environment where patients, families, employees and community are treated with courtesy and respect. We support an inclusive environment that nurtures the talents, skills and abilities of each individual to embody and reflect our core values: Innovation, Integrity, Teamwork, Commitment, Compassion and Respect.</p><p></p><p><b>
Grant Funding</b></p><p>
This is a grant-funded position. Compliance with funding requirements such as time and effort reporting, grant deliverables, and contract deliverables is required.</p><p></p><p><b>
E-Verify Employer</b></p><p>
Health Research Inc. (HRI) Roswell Park Division participates in the E-Verify program.</p></div>

University of Massachusetts

<div>Overview:
<p>
Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.</p>
Responsibilities:
<ul><li>Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA</li><li>
Identify, schedule and/or conduct participant study visits, interviews, and tests</li><li>
Coordinate participant remuneration/compensation per protocol</li><li>
Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors</li><li>
Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance</li><li>
Document and collect data and/or samples for research related procedures performed during participant study visits.</li><li>
Ensure clinicians and/or PI accurately document their study activities according to protocol</li><li>
Track and maintain study enrollment and completion of milestones</li><li>
Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe.</li><li>
Track and maintain study related information in the data management system within the required timeframe</li><li>
Responsible for monitoring the inventory of research related supplies</li><li>
Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board (IRB) processes</li><li>
Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs</li><li>
Present study status reports related to assigned research projects</li><li>
Participate in the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)</li><li>
Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.</li><li>
Comply with all safety and infection control standards appropriate to this position</li><li>
Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives</li><li>
Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices</li><li>
Must practice discretion and adhere to school and hospital confidentiality at all times</li><li>
Perform other duties as required.</li></ul>
Qualifications:
<ul><li>Bachelor&rsquo;s degree in a scientific or health related field, or equivalent experience</li><li>
0-1 year of related experience</li><li>
Ability to travel off site locations</li></ul>
Additional Information:
<div>
Usual office environment, laboratory, medical, surgical, and off campus study sites</div></div>

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