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Senior Clinical Study Manager
1 semana atrás
About the Role
We are seeking an experienced and skilled Senior Clinical Study Manager to join our site contracts department. As a key member of our team, you will be responsible for managing and executing clinical study agreements with sites worldwide.
Key Responsibilities
- Negotiate and finalize clinical study agreements (CSAs) on a study-by-study basis, ensuring compliance with company standards and industry regulations;
- Collaborate with global teams to develop and implement contract execution strategies, including forecasting site-specific contractual execution timelines;
- Provide expert guidance and support to internal and external stakeholders on CSA-related matters, including issue resolution and escalation procedures;
- Develop and maintain strong relationships with sponsors, investigators, and other stakeholders to ensure successful negotiation and execution of CSAs;
- Stay up-to-date with industry trends, regulatory requirements, and best practices in site contracting and negotiations.
Requirements
- Bachelor's degree in a life science or related field;
- Minimum 5 years of experience in CRO/pharmaceutical industry, preferably in clinical trial management or site start-up;
- Strong knowledge of applicable regulations, drug development, and clinical project management procedures;
- Excellent communication, negotiation, and problem-solving skills;
- Ability to work independently and collaboratively as part of a global team.
