Were working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full clinical trial lifecycle.
Key Responsibilities
- Lead clinical trials from study start-up through closeout
- Manage sponsor relationships and cross-functional project teams
- Oversee timelines, budgets, risks, and study deliverables
- Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance
- Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs
- Drive project success through effective communication, planning, and problem-solving
Requirements- Minimum 5 years of experience within a CRO
- Proven experience managing all aspects of clinical trials
- Hands-on knowledge of Data Management, Quality Control, and Clinical Operations- Strong understanding of ICH-GCP and regulatory requirements
-Clinical and Biometrics Project Management experience
- Excellent project management and stakeholder management skills
If interested please apply with your updated CV and Ill be in touch within 48 hours