Research Contract Specialist – Clinical Research Management

Prisma Health

Research Contract Specialist managing and negotiating clinical research agreements for Prisma Health. Ensuring regulatory compliance, timely execution, and consistency across research documents.

Posted 8/4/2026full-timeRemote • South Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in contract administration and research compliance, with a strong ability to interpret legal and regulatory language. Proficient in managing contractual agreements within clinical research settings while collaborating effectively with diverse stakeholders.

Highest-signal resume keywords

Contract AdministrationClinical ResearchRegulatory ComplianceContract Management SoftwareAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract ReviewLegal InterpretationResearch Agreement NegotiationMetrics ReportingClinical Trials Knowledge

Soft Skills

CollaborationRisk ManagementCommunication

Tools & Technologies

Project Management SoftwareContract Management Software

Industry Keywords

HIPAAAccreditation RequirementsResearch Support Services

About the role

Key responsibilities & impact

Report directly to the Director of Clinical Research Management and functionally to the Office of Legal Affairs
Facilitate timely review and execution of research-related contractual agreements on behalf of Prisma Health
Review and edit research-related agreements according to policy and relevant law, regulation, and accreditation requirements
Communicate edits, negotiate, and execute agreements with research staff and research sponsor staff
Respond to research staff contract inquiries
Use contract management and project management software to track contract activity and report metrics
Meet with internal institutional stakeholders, including Legal Affairs, Information Technology, and Purchasing, to review specialized contract issues and receive direction on regulatory requirements
Coordinate and communicate with Office of Research Support Services teams regarding contract priorities, policy changes, and other issues
Review clinical research documents for consistency of terms
Perform other duties as assigned

Requirements

What you’ll need

Bachelor's degree in Business, Legal, or related field of study
Two years of research, contract administration, or related experience
Attention to detail and accuracy
Ability to interpret legal and regulatory language
Collaborative approach with diverse stakeholders
Ability to balance speed with risk management
Working knowledge of contract or project management software preferred
Working knowledge of clinical trials, clinical research, and HIPAA preferred

Benefits

Comp & perks

Remote work supported from select states
Day shift