Clinical Research Coordinator/ Madison, WI (On-Site)
Fortrea · Madison, WI
Clinical OperationsFull timeCompany career page
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Role summary
Fortrea, a major clinical research organization, seeks a Clinical Research Coordinator for its Madison, Wisconsin site to manage early-phase trial operations. The role involves direct participant interaction, protocol review, study coordination, and collaboration with internal teams and sponsors on Phase 1 drug development studies.
What they're looking for
- Ability to read and comprehend clinical research protocols
- Experience working in fast-paced, team-oriented clinical environments
- Strong organizational and communication skills for multi-stakeholder coordination
- Capability to manage complex study operations and regulatory compliance
- Attention to detail for protocol adherence and documentation accuracy
What you'll be doing
- Oversee operational conduct of assigned studies with accountability for regulatory and protocol compliance
- Coordinate study critical events including check-ins, pharmacokinetic days, and participant check-outs while monitoring safety
- Prepare study documentation, schedules, and clinical procedure plans during set-up phase
- Facilitate study planning meetings and communicate with Project Managers, Investigators, and site staff
- Verify participant eligibility, manage study master files, and coordinate sample shipping and monitoring visits
Privacy & handoff
This role links to Fortrea's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.