Clinical Trial Manager
Listed on 2026-03-01
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Healthcare
Clinical Research, Medical Science
Job Overview
As a Clinical Trials Manager, you’ll lead the planning and execution of Phase 1–3 clinical studies and open-label extensions. You’ll manage CROs, vendors, and clinical sites to ensure trials are delivered on time, within budget, and in full compliance with GCP and regulatory standards.
PrimaryJob Responsibilities
- Oversee study timelines, budgets, and vendor performance
- Lead site and vendor qualification and selection
- Contribute to protocol, ICF, and study document development
- Coordinate drug supply forecasting and delivery
- Support data review and database lock activities
- Identify and mitigate study risks
- Ensure audit readiness and documentation compliance
- Collaborate cross-functionally to meet Clinical Development Plan goals
Job Requirements
- 4–6 years in clinical operations (biotech, pharma, or CRO)
- Experience managing multiple clinical trials and site visits
- Strong knowledge of ICH-GCP and drug development
- Bachelor’s degree in a scientific or healthcare field preferred
- Rare disease and neurology experience a plus
- Proficient in Microsoft Office and MS Project
- Excellent communication, organization, and problem-solving skills
Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals.
We will not share your information with anyone without your direct prior consent.
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