CMC Project Manager

Oxford, UK | Hybrid (1–2 days on site per week)

Are you ready to take full ownership of projects that will shape the future of oncology therapeutics? We’re looking for a CMC Project Manager who can hit the ground running, thrive in a collaborative environment, and bring real impact to a growing Biotech organisation in Oxfordshire.

This is your chance to work at the cutting edge of drug development, partnering with talented scientists and industry experts while driving critical CMC programmes forward.

Responsibilities:

• Leading CMC projects from start to finish – planning, execution, delivery and everything in between.

• Acting as the driving force between internal teams (Preclinical, Clinical, Regulatory, CMC and Quality) and external CDMO partners.

• Managing vendor relationships, budgets, timelines and risks to keep high-priority programmes moving smoothly.

• Supporting regulatory submissions and ensuring quality standards are met.

• Being a key member of the Project Management Office, sharing learnings, improving processes and ensuring best practice.

Background required:

• A background in Life Sciences (degree or equivalent).

• Solid experience as a Project Manager within Biotech/Pharma.

• Hands-on knowledge of CMC projects, ideally with exposure to small molecules.

• Direct experience working with CDMOs – you understand the challenges and how to navigate them.

• A proactive, confident communicator who can work cross-functionally and independently.

• PM qualifications (e.g. PMP) and regulatory/cGMP knowledge would be a bonus.

Why join?

• Be part of a team that’s expanding its CMC capability at a crucial stage of growth.

• Work in a hybrid model – typically 1–2 days in office.

• Enjoy a comprehensive benefits package including discretionary bonus, pension, life insurance, private healthcare and 25 days holiday (plus bank holidays).

If you’re looking for a role where you can make a tangible difference from day one – this could be the perfect next step in your career.

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