research data coordinator

Cleveland Clinic

<div></div><div><div>Join the Cleveland Clinic Florida team at the Krupa Center in Weston, where you will work alongside highly skilled and compassionate caregivers and board-certified family practice physicians to provide patient-first healthcare. Cleveland Clinic is consistently recognized as one of the top hospitals in the nation, offering quality preventive care, management of chronic conditions and comprehensive services for the entire family. At Cleveland Clinic, you will receive strong support and recognition, collaborate with dedicated professionals and build a rewarding career with one of the world&rsquo;s most respected healthcare organizations. 
As a Research Coordinator II for DDI, you play a critical role in documenting data, maintaining timely reports, preparing audits, and ensuring departmental compliance, directly supporting Cleveland Clinic&rsquo;s mission to conduct safe, ethical, and efficient research. In this role, you will serve as the operational backbone of the research program, protecting patients, maintaining protocol integrity, and ensuring meaningful outcomes. The program focuses on improving quality of life after cancer surgery and prioritizes patient-centered research, partnering with patients to incorporate their insights into study design and enhance the overall patient experience.
A caregiver in this role works days from 8:30 a.m. - 5:00 p.m.
A caregiver who excels in this role will:<ul><li>
Coordinate the compliant implementation and conduct of human subject research projects.
</li><li>Maintain regulatory documents and binders, conduct data management, complete IRB submissions and communicate with the research team.
</li><li>Report and complete serious adverse events and/or safety logs.
</li><li>Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance.
</li><li>Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
</li><li>Schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
</li><li>Plan, conduct and evaluate project protocols and research subject recruitment.
</li><li>Monitor and report project status and research data.
</li><li>Complete regulatory documents, data capture, monitoring plans and protocol-related activities.
</li><li>Assist with preparing and responding to audits and maintaining research tools.
</li></ul>Minimum qualifications for the ideal future caregiver include:<ul><li>
High School Diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I</li><li>
OR Associate's or Bachelor's degree in health care or science related and one year of experience as a Research Coordinator I or performing the role of a Research Coordinator I</li><li>
Proficient with computer-based skills such as word processing, spreadsheets, database and presentation software</li><li>
Understand basic concepts of study design</li></ul>
Preferred qualifications for the ideal future caregiver include:
<ul><li>Associate or Bachelor's degree in health care or science related field</li><li>
Experience as a clinical research coordinator</li></ul>
Physical Requirements:<ul><li>
Ability to perform work in a stationary position for extended periods</li><li>
Ability to operate a computer and other office equipment</li><li>
Ability to communicate and exchange accurate information</li><li>
In some locations, ability to move up to 25 pounds</li></ul>
Personal Protective Equipment:<ul><li>
Follows standard precautions using personal protective equipment as required.</li></ul></div><div>
Pay Range
Minimum Annual Salary: $47,530.00
Maximum Annual Salary: $72,475.00
The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate&rsquo;s actual compensation will be determined after taking factors into consideration such as the candidate&rsquo;s work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic&rsquo;s benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).</div></div>

Research Coordinator II

UT Southwestern Medical Center

WHY UT SOUTHWESTERN?
 With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report , we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!
 
JOB SUMMARY
 Works under the direction of an Investigator(s) with general supervision, to provide ongoing data management for local and national research studies and may coordinate observational (non-treatment/treatment) trials/studies. May provide supporting role for more complex studies under the direction of the PI, Clinical Research Coordinator and/or Clinical Research Lead.
 
Key responsibilities include understanding visit schedules; assisting research staff; reviewing and abstracting medical record information; entering data into case report forms; supporting data queries and regulatory data compilation; maintaining databases; performing QA/QC checks; preparing annual reports and research records; recruiting and enrolling study participants; assisting with patient care tasks; managing research supplies; and performing other assigned duties.
 BENEFITS
 UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:
 PPO medical plan, available day one at no cost for full-time employee-only coverage
 100% coverage for preventive healthcare-no copay
 Paid Time Off, available day one
 Retirement Programs through the Teacher Retirement System of Texas (TRS)
 Paid Parental Leave Benefit
 Wellness programs
 Tuition Reimbursement
 Public Service Loan Forgiveness (PSLF) Qualified Employer
 Learn more about these and other UTSW employee benefits!
 
EXPERIENCE AND EDUCATION
 
Required
 Education
 High School Diploma or
 Associate's Degree in medical or science related field or
 Bachelor's Degree medical or science related field and no prior experience
 
Experience
 2 years experience with High School Diploma or
 1 year experience with Associate's Degree
 
Preferred
 Licenses and Certifications
 (BLS) BASIC LIFE SUPPORT may be required based on affiliate location requirements.
 (CPRAED) CPR AED may be required based on affiliate location requirements.
 
JOB DUTIES
 Understands visit schedules, criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.
 Assists research staff by completing research protocol related tasks.
 Reviews and abstracts information from medical records including eligibility criteria.
 Enters data into case report forms or other data collection system based on research study. Assists with maintenance of study level documentation.
 Assists with data queries and possible edits for accuracy.
 Compiles data for regulatory requirements and /or deadlines for local or sponsor submissions.
 Maintains existing databases and ensures data integrity.
 Performs QA/QC clinical analysis and data checks using various databases based on trial.
 Assists with preparing annual reports and/or modifications to institutional review board (IRB). This may include reportable events (UPIRSO).
 Assist and prepare research records for formal sponsor audits or internal audits.
 Recruits and enrolls patients in research study that may include consenting patients after training and with supervision.
 With adequate training and supervision, assists with participant screening and recruitment for more complex trials.
 Conducts and documents consent for participants in studies. Assists with the development of consent plans and documents for participants.
 Identifies incomplete, inaccurate, or missing data for more complex studies and works with lead coordinator to correct errors.
 Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment is in good working order.
 With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.
 Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).
 With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG's needed for research study. Based on research study, other procedures/equipment/services may be required.
 May perform patient care (basic skills) under the direction of PI following scope of work document.
 Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
 Performs other duties as assigned.
 SECURITY AND EEO STATEMENT
 
Security
 This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
 
EEO
 UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

Clinical Research Assistant II, Internal Medicine Digestive and Liver

The START Center for Cancer Research

<div>The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering &quot;Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.
 We are seeking a CTMS Entry Coordinator. This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
Work Schedule: Monday-Friday, 8am-5pm
Location: Myrtle Beach, SC
 Essential Responsibilities<ul><li>
Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs.
</li><li>Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.</li><li>
Contact patients in follow-up as needed per protocol.</li><li>
Review and utilize protocols as guides for study activities for assigned studies.</li><li>
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.</li><li>
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.</li><li>
Ensure that data transmissions remain current for assigned studies.</li><li>
Provide support and information to onsite and remote monitors as necessary.</li><li>
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.</li><li>
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.</li><li>
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.</li><li>
Communicate as needed with accounts receivable staff regarding transmitted data.</li><li>
Other duties may be assigned at any time.</li></ul> 
 Required Education and Experience:<ul><li>
High School diploma or equivalent.</li><li>
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.</li><li>
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.
</li><li>Familiarity with medical terminology.</li><li>
Strong organizational skills and a sense of timeliness in completing projects.</li><li>
Must be detail-oriented and able to understand instructions and work independently.</li></ul>
 Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:
<ul><li>401(k) retirement savings plan with employer match</li><li>
Eligibility for an annual performance bonus, based on role and company results</li><li>
Generous paid time off and paid holidays</li><li>
Comprehensive medical, dental, and vision coverage and optional insurance options</li><li>
Company‑paid life and disability insurance for added financial protection</li><li>
Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one</li><li>
Flexible FSA and HSA plans to support your financial wellness</li><li>
Commitment to a supportive environment that values balance, wellbeing, and flexibility</li><li>
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.</li></ul>
 More About START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history.
 Learn more at STARTresearch.com.
 Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.</div>

CTS Entry Coordinator

Alcanza Clinical Research

<div>
 
 Department:
 
 Operations
 
 
 
 Location:
 
 North Georgia Clinical Research
 
 
 
 Description
 
 
 
 Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
 
 
 The
 
 Data Entry Coordinator
 
 works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
 
 
 
 Key Responsibilities
 
 
 
 
 Essential Job Duties:
 
 
 
 
 Responsibilities
 
 
 
 In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems. Responsibilities may include but are not limited to:
 
 
 <ul>
 <li>
 Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software
 </li>
 <li>
 Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements
 </li>
 <li>
 Reporting any irregularities or problems with a study to the appropriate parties
 </li>
 <li>
 Supporting other clinical research-related activities
 </li>
 <li>
 Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines
 </li>
 <li>
 Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.
 
 
 </li>
 </ul>
 
 Skills, Knowledge And Expertise
 
 
 
 
 Minimum Qualifications
 
 : High School diploma or equivalent and a minimum of 1 year of clinical data entry experience, or an equivalent combination of education and experience.
 
 
 
 Required Skills
 
 
 
 <ul>
 <li>
 Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm);
 </li>
 <li>
 Strong organizational skills and attention to detail.
 </li>
 <li>
 Well-developed written and verbal communication skills.
 </li>
 <li>
 Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
 </li>
 <li>
 Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
 </li>
 <li>
 Must be professional, respectful of others, self-motivated, and have a strong work ethic.
 </li>
 <li>
 Must possess a high degree of integrity and dependability.
 </li>
 <li>
 Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 <ul>
 <li>
 Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
 </li>
 <li>
 Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
 </li>
 </ul>
</div>

Healthcare Data Entry Coordinator

Research Center

Job DescriptionThe Data Entry Coordinator is responsible for the submission of all clinical trial data, ensuring accuracy and integrity of files. Keeps track of received subject visits data and enters it into the Electronic Data Capture systems within the agreed time frame. Informs Principal Investigator and study coordinators about the status of the clinical database, guaranteeing database lock readiness and completeness. All duties are carried out in accordance with the company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable Local, State, and Federal regulationsJob Functions<ul><li>Critically evaluates clinical data for accuracy and completeness, while ensuring the safety and confidentiality of participants, according to the study monitoring plans.</li><li>Submits research data into Electronic Data Capture systems (EDC) within the established timelines.</li><li>Resolves and escalates queries to the research team.</li><li>Performs data-related corrections in eCRFs when applicable.</li><li>Periodically performs quality control of EDC systems focused on data integrity/accuracy and database lock readiness.</li><li>Proofreads and verifies data entered.</li><li>Updates internal Database and generates reports using dedicated software (Trust).</li><li>Assists Clinical Research Coordinators in the creation of source documents, identifying discrepancies or missing data, based on EDC requirements, blank eCRFs, and EDC Guidelines.</li><li>Provide updates on the status of all data entry-associated tasks to the Data Entry Manager.</li><li>Create and document queries and findings in the Trust system arising from datareviews performed for future analysis and retraining as necessary.</li><li>Notify the Data Entry Manager of significant findings from the collected subjectdata that may greatly impact the quality and integrity of the data.</li><li>Upload the laboratory results to the Trust system for review by the clinical teamand the Investigators.</li><li>Completes additional tasks as required by specific study protocols or as assignedby the Data Entry Manager.</li><li>Process electronic medical records and update the Trust system.</li><li>Perform quality control on the data gathered by the Clinical Team, evaluating its completeness, accuracy, and compliance with ALCOA+ standards, as well as the requirements set forth by the Sponsor. Additionally, ensure adherence to the Study Protocol and associated Guidelines.</li></ul>QualificationsSkills<ul><li>Must have high attention to detail and accuracy with the ability to read and follow instructions.</li><li>Excellent communication, interpersonal and organizational skills.</li><li>Demonstrated understanding of HIPAA confidentiality regulations.</li><li>Demonstrated understanding of medical terminology.</li><li>Proficient computer skills including proficient keyboarding skills and experience in using Microsoft Office products, electronic mail and/or electronic health information records systems.</li><li>Ability to work independently and collaboratively within a team environment.</li><li>Demonstrated strong problem solving skills including the ability to handle difficult situations. Ability to prioritize workload and work under pressure in a fast-paced environment with time constraints.</li></ul>Qualifications:<ul><li>Works well in a team environment.</li><li>Familiarity with Clinical Terminology preferred.</li><li>Excellent written and verbal communication skills.</li><li>High attention to detail and organization.</li><li>Clinical Research experience required.</li><li>Bi-lingual English/Spanish preferred.</li><li>Ability to work after hours and weekends if needed.</li><li>Knowledge of Microsoft Office 365.</li><li>Ability to type 40+ WPM with complete accuracy and proficiency.</li></ul>Education/Experience<ul><li>A Bachelor degree or equivalent is required, and relevant formal academic/vocational qualification, and/ or an associate degree in a medical or information technology field, is preferred.</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years) or equivalent combination of education, training, and experience.</li><li>Experience in medical coding.</li><li>Experience in word processing, spreadsheets, databases systems, and Microsoft Office required.</li></ul>Work schedule:<ul><li>Monday to Friday &ndash; 8:00 am &ndash; 4:30 pm, unless otherwise indicated</li></ul>Benefits offered:<ul><li>Medical, Dental, and Vision Insurance</li><li>Life Insurance (includes Will Preparation, Employee Assistance Program (EAP), and Travel Assistance)</li><li>Short &amp; Long-Term Disability</li><li>Workers&rsquo; Compensation Insurance</li><li>COBRA Continuation Coverage</li><li>401(k) Retirement Savings Plan with employer match</li><li>Paid Time Off (PTO)</li><li>Paid Holidays</li><li>Bereavement Leave</li><li>Family and Medical Leave Act (FMLA)</li><li>Military Leave</li><li>Referral Program</li><li>Tuition Assistance/Professional Development</li><li>Certification Reimbursement</li></ul>Job Type: Full-timePay: $20.00 - $26.00 per hourBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Professional development assistance</li><li>Referral program</li><li>Vision insurance</li></ul>Experience:<ul><li>Clinical research: 2 years (Preferred)</li></ul>Work Location: In person

Data Entry Clinical Research

Thomas Jefferson University & Jefferson Health

<div>Job Details
Works under direct supervision and assists research coordinators with organizing, gathering and compiling clinical research data. Tracks and maintains credentialing documentation for staff and all researchers participating in clinical trials in accordance with IRB regulations. May provide clerical and technical support to ensure adherence to research protocols and quality of information received.
Job Description
<ul><li>Performs a variety of research, data base and clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.
</li></ul><ul><li>Organizes and maintains documentation required for clinical trial(s).
</li></ul><ul><li>Informs Principal Investigator and/or designated individual on any issues concerning patient&rsquo;s response to treatment/medication/ any adverse effects overall to patients.
</li></ul><ul><li>Assists Principal Investigator with IRB filings and annual reviews.
</li></ul><ul><li>May assist in the enrollment of human subjects.
</li></ul>Minimum High School Diploma or equivalent.
AND
Experience:
Experience in research or clinical setting preferred.
Work Shift
Rotating (United States of America)
Worker Sub Type
Regular
Employee Entity
Thomas Jefferson University
Primary Location Address
132 S 10th Street, Philadelphia, Pennsylvania, United States of America
Nationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University , home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students. Jefferson Health , nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at 32 hospitals campuses and more than 700 outpatient and urgent care locations throughout the region. Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range of health coverage options in Pennsylvania and New Jersey for more than 35 years.
Jefferson is committed to providing equal educational and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.
Benefits
Jefferson offers a comprehensive package of benefits for full-time and part-time colleagues, including medical (including prescription), supplemental insurance, dental, vision, life and AD&amp;D insurance, short- and long-term disability, flexible spending accounts, retirement plans, tuition assistance, as well as voluntary benefits, which provide colleagues with access to group rates on insurance and discounts. Colleagues have access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service. All colleagues, including those who work less than part-time (including per diem colleagues, adjunct faculty, and Jeff Temps ), have access to medical (including prescription) insurance.
For more benefits information,</div>

Clinical Research Assistant (Part Time | Pharmacology/Experimental Therapeutics)

WHY UT SOUTHWESTERN?
 With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report , we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!
 
JOB SUMMARY
 Works under the direction of an Investigator(s) with general supervision, to primarily provide ongoing data management for local and national research studies. May coordinate observational (non-treatment) studies.
 
The position will assist with data entry, documentation, database maintenance, accuracy checks, regulatory submissions, study visit coordination, and protocol related tasks. It will also support IRB reporting, patient recruitment and enrollment, supply management, and with proper training specimen collection and basic study procedures such as vitals, phlebotomy, and EKGs. Duties may involve direct interaction with patients or research participants and handling of medical or research records, along with other assigned research tasks.
 BENEFITS
 UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:
 PPO medical plan, available day one at no cost for full-time employee-only coverage
 100% coverage for preventive healthcare-no copay
 Paid Time Off, available day one
 Retirement Programs through the Teacher Retirement System of Texas (TRS)
 Paid Parental Leave Benefit
 Wellness programs
 Tuition Reimbursement
 Public Service Loan Forgiveness (PSLF) Qualified Employer
 Learn more about these and other UTSW employee benefits!
 
EXPERIENCE AND EDUCATION
 
Required
 Education
 High School Diploma or GED
 
Preferred
 Licenses and Certifications
 (BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements.
 (CPRAED) CPR AED may be required based on affiliate location requirements
 
JOB DUTIES
 Enters data into case report forms or other data collection system based on research study. Assists with maintenance of study level documentation.
 Assists with data queries and possible edits for accuracy.
 Compiles data for regulatory requirements and /or deadlines for local or sponsor submissions.
 Maintains existing databases and ensures data integrity.
 Understands visit schedules, criteria and protocol requirements for routine and low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.
 Assists research staff by completing research protocol related tasks.
 Assists with preparing annual reports and/or modifications to institutional review board (IRB). This may include reportable events (UPIRSO).
 Reviews and abstracts information from medical records including eligibility criteria.
 Recruits and enrolls patients in research study that may include consenting patients after training and with supervision.
 Assists with ordering and maintaining research supplies following university/department procedures, ensuring that equipment is in good working order.
 With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols.
 Assists in preparing studies for closeout, (e.g. packing files, documenting files for storage, shipping extra supplies back to sponsor).
 With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKG's needed for research study. Based on research study, other procedures/equipment/services may be required.
 Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
 Performs other duties as assigned.
 SECURITY AND EEO STATEMENT
 
Security
 This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
 
EEO
 UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

Clinical Research Assistant I, Internal Medicine Digestive and Liver

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