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About the role
Key responsibilities & impact- Engage in extensive training with senior Clinical Research Associates and Managers
- Conduct clinical monitoring visits in accordance with study protocol and regulations
- Suggest ideas to improve site recruitment plans
- Create and maintain appropriate documentation regarding site management
- Manage the progress of assigned studies by tracking regulatory submissions and approvals
Requirements
What you’ll need- Clinical research coordination experience at site level
- Nursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences
- Knowledge of electronic data capture preferred
- Ability to travel approximately 65%-85%, domestic or international, as required.
Benefits
Comp & perks- health and welfare benefits
- overtime compensation
- bonuses
- incentive plans
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical research coordinationsite managementregulatory submissionsstudy protocol complianceelectronic data capture
Soft Skills
communicationorganizationalproblem-solvingcollaboration
