Freelance Regional Clinical Trial Manager
Rho
contract
Posted on:
Location Type: Remote
Location: Poland
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Tech Stack
About the role
- Oversee the planning, initiation, execution, and closure of clinical trials within your region
- Ensure compliance with GCP, FDA, and other applicable regulatory requirements
- Manage site selection, initiation, monitoring, and closing activities
- Collaborate with cross-functional teams to ensure efficient and effective trial operations
- Monitor trial progress and troubleshoot issues that may arise, providing timely solutions
- Develop and maintain strong working relationships with investigative sites and teams
Requirements
- Degree in a related field (life sciences, nursing, etc.) with at least 5 years of experience in clinical trial management, preferably in a CRO or pharmaceutical environment.
- Proven experience managing regional or multi-site clinical trials successfully.
- Strong communicator with excellent written and verbal skills in English; knowledge of additional languages is an advantage.
- Detail-oriented with a commitment to quality and ethical conduct in clinical trials.
- High-Character: Collaborate with honesty and integrity; shown ability to build trust and work well within a team environment.
- Effective problem-solving and critical thinking skills, with the ability to adapt quickly to changing environments.
- Willingness to travel and have a valid driver’s license.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial managementGCPFDA compliancesite selectionmonitoring activitiestrial executiontrial closureproblem-solvingcritical thinkingdetail-oriented
Soft Skills
strong communicatorexcellent written skillsexcellent verbal skillscollaborationintegritytrust-buildingteamworkadaptabilitycommitment to qualityethical conduct