Soc/Clin Research Assistant
About The Position
This position will serve as a Study Coordinator maintaining the continuity, integrity, and productivity of four active research studies under the direction of Dr. Elizabeth Andersen and Dr. Chris Sikes-Keilp in the Department of Psychiatry in the School of Medicine. The Study Coordinator will directly support all aspects of research procedures, including data collection and management, recruitment, scheduling, and participant tracking in accordance with federal and institutional guidelines. This role is critical for maintaining participant safety, managing communication with adolescent participants and their families, and ensuring that clinical assessments and biological sample collection occur reliably and on schedule. The study coordinator will be responsible for recruitment, scheduling enrollment and lab visits, tracking participant compliance, data management and regulatory oversight for 4 active studies (2 that are clinical trials). They will also be responsible for administering lab sessions and supervising other staff and students.
Requirements
- Experience in research procedures.
- Experience in data collection and management.
- Experience in recruitment and scheduling.
- Experience in participant tracking.
- Knowledge of federal and institutional guidelines for research.
- Ability to maintain participant safety.
- Ability to manage communication with adolescent participants and their families.
- Ability to ensure clinical assessments and biological sample collection occur reliably and on schedule.
- Experience in administering lab sessions.
- Experience in supervising other staff and students.
Responsibilities
- Maintain continuity, integrity, and productivity of four active research studies.
- Support all aspects of research procedures, including data collection and management.
- Manage recruitment, scheduling, and participant tracking.
- Ensure participant safety.
- Manage communication with adolescent participants and their families.
- Ensure clinical assessments and biological sample collection occur reliably and on schedule.
- Schedule enrollment and lab visits.
- Track participant compliance.
- Perform data management and regulatory oversight for 4 active studies (2 clinical trials).
- Administer lab sessions.
- Supervise other staff and students.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
