Research Assistant

POSITION OBJECTIVE

Working with a high degree of independence and under general direction, coordinate major activities in medical and related technical areas. The Clinical Research Coordinator coordinates and manages the major administrative and operational activities of the PROSPECT research registry and related studies. This position is responsible for day-to-day study coordination, participant administration, data and record management, and regulatory documentation to support the successful conduct of longitudinal human subjects research.

The PROSPECT registry is a multiyear longitudinal research program focused on individuals at risk for genetic prion disease. The position supports the research mission by ensuring accurate data collection, continuity of participant follow-up, coordination of external services, and compliance with institutional and regulatory requirements.

• Independently coordinate major administrative and operational activities of the PROSPECT research registry, including participant enrollment, scheduling, follow‑up tracking, and ongoing study maintenance. Assist in developing procedures, coordinate information with others as needed. (20%)
• Coordinate major activities of laboratory/ research and administer informed consent processes in accordance with approved protocols and institutional requirements, including remote consent using HIPAA‑compliant platforms. Ensure consent documentation is complete, accurate, and properly maintained. (10%)
• Coordinate and administer remote study assessments and participant‑reported data collection. Review submissions for completeness and accuracy and ensure appropriate documentation and data entry. (20%)
• Provide input and recommendation to principal investigator regarding significant developments in research projects, participant status, scheduling challenges, and administrative or procedural issues affecting research activities. Independently resolve routine issues to ensure continuity of study operations. (10%)
• Maintain, monitor, and reconcile research databases and records, ensuring accuracy, completeness, and timely updates of participant information, assessments, and longitudinal follow‑up data. Identify discrepancies and take corrective action as appropriate. Perform the most complex quantitative analytical procedures. (10%)
• Coordinate genetic testing and genetic counseling services with external vendors and participants, including scheduling, documentation, and follow‑up to ensure adherence to study timelines and requirements. (10%)
• Prepare, submit, and maintain regulatory and study documentation, including IRB submissions, continuing reviews, amendments, correspondence, and required reports. Ensure records are audit‑ready and compliant with institutional standards. (10%)
• Compile, organize, and summarize administrative and research data to support analysis, presentations, manuscripts, and reporting needs of the principal investigator and study team. Co‑author research projects. (10%)

• May supervise research assistants and students. Provide functional guidance, training, or work direction to student employees or temporary research staff as assigned. Teach or instruct others in research techniques. (5%)
• Order, track, and distribute study‑related supplies and materials. (5%)
• Perform other duties as assigned. (