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Clinical/Hc Research Associate
Company | University of Iowa |
Address | Iowa City, IA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-07-01 |
Posted at | 11 months ago |
The Department of Epidemiology in the College of Public Health is seeking a Clinical/HC Research Associate to participate in the design, execution, and control of clinical research trials; coordinate the processing and analysis of trials data; coordinate clinical trial protocols and procedures; and develop new and/or revised research methodologies for MOST (Multicenter Osteoarthritis Study).
- Coordinate services/referrals as appropriate with other departments participating in the clinical research as appropriate.
- Participate in the development of the general research goals and in the planning and implementation of the clinical trials.
- Organize clinic/study procedures, follow study participants, and manage collection of accurate data in a timely manner. Keeping data and documentation secure and confidential.
- Oversee operations of clinical research studies including the recruitment, coordination, and scheduling of subject participation and procedures per protocol requirements.
- Enter patients in the protocol, ensuring that all prerequisites have been completed and are within the required parameters.
- Assist in judging validity to data and make recommendations.
- Assist in the design, development, and execution and administration of protocols and clinical studies.
- Coordinate patient care needs and obtain follow up information from local physicians or laboratories or appropriate healthcare providers per established research protocols.
- Assist patients with problems related to their protocol therapy such as consultation when calling concerns related to: returning for emergency evaluation in the case of side effects, assisting with emotional problems or other related areas.
- Assist and/or direct others in obtaining patient consent to enter protocols and counsel patients and families regarding investigational therapy.
- Use evaluation data to revise and implement change.
- Perform complex statistical analysis of data and prepare data for computer analysis.
- Assist in the preparation of research papers and manuscripts for publication and presentation at conferences and workshops, and in the writing of project reports, articles and other documents for submission to study sponsors.
- Maintain records and services provided and work with individual protocol budgets.
- Collect and manage data in clinical trials using a variety of data programs including REDCap data capture.
- Serve as a liaison to local physicians/hospitals and collaborating institutions to facilitate care of protocol patients when hospitalized at outside institutions.
- Obtain documentation of the hospitalizations, as well as provide notification to the Principal Investigator, Study Sponsor and FDA as required per protocol.
- Provide administrative supervision.
- Serve as a liaison to identify exact patient tests and procedures which are paid for by study sponsors, and to assist with questions related to billing for protocol treatment procedures.
- Serve as a liaison to IRB committee. Prepare and submit IRB information for approval.
- Mentor new staff.
- Schedule: Full-time
- Work Modality Options: On Campus
- Classification Title: Clinical/HC Research Associate
- Appointment Type: Professional and Scientific
- Pay Level: 5A
- Contact Name: Michele Hogue
- Contact Email: [email protected]
- Organization: College of Public Health
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