Overview
The Research Contract Specialist will report directly to the Director of Clinical Research Management and have a functional reporting relationship to the Office of Legal Affairs. This role facilitates the timely review and execution of research-related contractual agreements.
Remote work is supported from select states.
Responsibilities
- Review and edit research-related agreements in accordance with policy, law, regulation, and accreditation requirements.
- Communicate edits, negotiate, and execute agreements with research staff and research sponsor staff in a timely manner.
- Respond to contract inquiries from research staff.
- Use contract management and project management software to track contract activity and report on metrics.
- Meet with internal stakeholders (Legal Affairs, Information Technology, Purchasing, etc.) to review specialized contract issues and receive direction on regulatory requirements.
- Coordinate and communicate with the Office of Research Support Services teams regarding contract priorities, policy changes, and other issues.
- Review clinical research documents to ensure consistency of terms.
- Perform other duties as assigned.
Requirements
- Bachelor's degree in Business, Legal, or related field.
- Minimum of two (2) years of experience in research, contract administration, or related fields.
Knowledge, Skills, and Abilities
- Strong attention to detail and accuracy.
- Ability to interpret legal and regulatory language.
- Collaborative approach with diverse stakeholders.
- Ability to balance speed with risk management.
- Preferred working knowledge of contract or project management software.
- Preferred working knowledge of clinical trials, clinical research, and HIPAA.
Work Shift
- Day shift (United States of America)
Location
- Greenville Memorial Hospital
Department
- Research Services - Clinical Research Management