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Research Project Manager
1 week ago
Join our team as a Clinical Study Manager and take on the challenge of overseeing complex clinical studies.
About the Job- This role requires a strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Responsibilities include managing clinical research tasks, collaborating with service providers, and ensuring data quality.
- The successful candidate will contribute to the development of core study documents, facilitate timely reporting, and collaborate with Valneva stakeholders.
Our ideal candidate has a Master's degree in Life Science or equivalent experience, preferably with 5+ years in clinical trials management. Strong organizational skills, IT proficiency, and fluency in English are essential.
Key Responsibilities- Manage roles and responsibilities of service providers
- Contribute to the development of core study documents
- Ensure data quality and compliance with protocols
- Collaborate with Valneva stakeholders to monitor budgets and financial agreements
