About the Role
Our client, a leading entity in the Life Sciences sector, is seeking an accomplished Senior Project Manager for their base in Cambridge . This crucial role involves managing complex research, development, and manufacturing projects, adhering to stringent regulatory and quality standards. You will lead dedicated teams, ensuring the successful execution of projects that advance scientific innovation and patient well-being. This is a highly rewarding opportunity for a dedicated project manager to make a substantial impact within a world-renowned scientific hub.
Key Responsibilities
- Oversee the planning, execution, and delivery of projects within the life sciences domain, including drug development and manufacturing.
- Develop comprehensive project plans, managing scope, timelines, budgets, and resources effectively.
- Ensure strict adherence to GxP guidelines, regulatory requirements (e.g., FDA, EMA), and quality management systems.
- Collaborate closely with R&D, clinical, regulatory affairs, and manufacturing teams to achieve project objectives.
- Manage project risks, issues, and dependencies, implementing robust mitigation strategies.
Requirements
- Minimum of 8 years of experience in project management , with a significant focus on the life sciences or pharmaceutical industry .
- Proven track record of managing complex R&D, clinical trial, or manufacturing projects.
- Strong understanding of regulatory affairs, quality assurance, and GxP environments.
- Excellent leadership, communication, and stakeholder management skills.
- PMP or PRINCE2 certification, along with a relevant scientific degree, is highly desirable.
Benefits
- Competitive salary package and attractive bonus opportunities.
- Comprehensive private health insurance, dental, and vision coverage.
- Relocation assistance may be provided.
- Opportunities for continuous professional development and advancement within the sector.
- A scientifically stimulating and collaborative work environment at the forefront of innovation.
