Clinical Study Manager
4 days ago
Pfizer is seeking a highly skilled and experienced professional to join our medical team as a Site Care Partner. This role will play a critical part in managing clinical studies, ensuring they are completed within time, budget, and scope.
Key Responsibilities- Develop and manage plans to achieve objectives, interpreting internal and external business challenges and recommending best practices for improvements.
- Manage complex project environments, anticipating and troubleshooting roadblocks and influencing teams to achieve targets for the division.
- Work proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery.
- Forecast and manage the Clinical Trial Budget for the program.
- Provide country and regional level input to country outreach surveys.
- Create awareness by working as a cross-functional Team Leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external.
- Bachelor's Degree
- 7+ years' experience in the pharmaceutical industry
- Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations
- Demonstrated project management/leadership experience
- Experience with CRO oversight
- Ability to evaluate, interpret, and present complex issues and data to support risk
- Excellent communication skills, both written and verbal; must be fluent in English
Pfizer offers a range of great benefits for our colleagues, including paid parental leave, access to health and wellness apps, career growth experiences, recognition and rewards, paid volunteer days, life insurance benefits, and more.
We are committed to diversity, equity, and inclusion and offer engagement opportunities in our Colleagues Resource Groups (CRGs) and workstreams.
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Clinical Study Manager
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