Project Manager, CGT and Biologics Bioanalytical Services

About the role:

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) supporting drug discovery through to manufacturing with fully integrated high-quality services. We support 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases, working with over 3,300 global customers.

What You'll Do

We are seeking a highly motivated and experienced Project Manager to join our team. As a Project Manager for CGT and Biologics Bioanalytical Services at Pharmaron, you will play a pivotal role in driving our business growth and establishing our leadership in the industry. Your primary focus will be on coordinating scientific account management for our specialized bioanalytical testing and in-vivo services for our scientific partners and companies developing CGT and Biologics treatments.

• Cultivate a deep understanding of Pharmaron's bioanalytical testing workflow, enhance familiarity with the regulatory requirements (GLP/GCLP/CLIA).
• Enhance knowledge of departmental capabilities, general technical procedures, equipment, and standard operating procedures.
• Project Planning: In collaboration with Study Directors, design projects that meet sponsors' needs in a scientifically sound and cost-effective manner.
• Provide scientific consultations for the clients to support Pharmaron services.
• Create compelling study proposals, including budgets and detailed project scopes.
• Maintain effective communication with clients, manage expectations, providing regular updates and addressing inquiries.
• Collaborate with cross-functional teams to ensure seamless project execution.
• Proactively identify and mitigate project risks.
• Maintain accurate and comprehensive project documentation including meeting agendas and minutes.

What We're Looking For

• Bachelor's Degree in biology, life sciences, pharmacology, or chemistry.
• Advanced degree (Master's or higher) is preferred.
• Proven experience in project management, preferably in the bioanalytical CRO.
• Strong understanding of regulatory requirements: GLP/GCLP, GMP, CLIA.
• Ability to independently draft study proposals, budgets, and project scope of work.
• Excellent organizational and multitasking skills.
• Effective communication skills for client interactions.
• Motivation to learn and adapt to evolving industry trends.

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry, founded in 2004 and investing in its people and facilities. We have a broad spectrum of research, development, and manufacturing service capabilities across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore, we have an excellent track record in delivering R&D solutions to our partners in North America, Europe, Japan, and China. Our collaborative culture, "Employees Number One" and "Clients Centered," fosters an inclusive and innovative environment. We offer a comprehensive benefits package including medical, dental, vision insurance, retirement plans, paid time off, and professional development opportunities.

How to Apply

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed.