Senior Clinical Project Manager
4 days ago
We are seeking a highly skilled and experienced Senior Clinical Project Manager to join our team at Pfizer. As a key member of our medical team, you will be responsible for managing clinical studies and ensuring that they are completed within time, budget, and scope.
Key Responsibilities- Develop and manage plans to achieve objectives, including project timelines and budgets.
- Lead complex projects across business units, developing and implementing strategies to drive success.
- Approve study startup, study monitoring, and protocol recruitment plans, ensuring alignment with business objectives.
- Resolve escalated issues identified by the site activation subteam, working in partnership with the Study Manager.
- Work proactively with Clinical Research Organizations (CROs) and data management functions to ensure alignment on data flow and timely delivery.
- Manage operational study management for one or more studies of limited complexity or a unique part of a larger study.
- Forecast and manage the clinical trial budget for the program, ensuring effective resource allocation.
- Provide country and regional level input to country outreach surveys, ensuring a comprehensive understanding of market trends.
- Create awareness by working as a cross-functional team leader to deliver site intelligence initiatives with various stakeholders, both internal and external.
- Approve and oversee drug supply management, ensuring the smooth flow of drug supply to sites.
- Participate in global initiatives to improve operational efficiencies, driving process improvements and best practices.
- Evaluate study progress reports and results, recommending corrective action or study termination for non-performance.
- Maintain regular communications with investigator sites, gathering status updates, informal and formal performance metrics, and study-level feedback.
- Bachelor's Degree in a relevant field.
- 7+ years' experience in the pharmaceutical industry, with a focus on clinical research and project management.
- Applicable pharmaceutical industry experience, including working knowledge of Good Clinical Practices, monitoring, clinical, and regulatory operations.
- Demonstrated project management/leadership experience, with a proven track record of delivering complex projects.
- Experience with CRO oversight, ensuring effective collaboration and data management.
- Ability to evaluate, interpret, and present complex issues and data to support risk management.
- Excellent communication skills, both written and verbal, with fluency in English.
- Effective decision maker, analytical, and solution-oriented, with a focus on driving business outcomes.
- Proficiency in Microsoft Office Suite, with a focus on project management tools and software.
- Master's degree in a relevant field.
- Broad-based experience in clinical research, with a focus on therapeutic areas and international experience.
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