CMC Project Manager

Next Phase Recruitment; England; On-site; GBP 50,000 - 70,000; Full time

Benefits offered by this job

Discretionary bonus

Pension

Life insurance

Private healthcare

25 days holiday plus bank holidays

Job summary

A leading recruitment firm is seeking a CMC Project Manager in Oxfordshire to lead projects shaping the future of oncology therapeutics. You will be responsible for managing CMC projects from planning to execution, collaborating with internal teams and external partners. The ideal candidate has a degree in Life Sciences and solid project management experience in Biotech/Pharma. This role offers hybrid working and a comprehensive benefits package.

Qualifications

• Solid experience as a Project Manager within Biotech/Pharma.
• Hands-on knowledge of CMC projects, ideally with exposure to small molecules.
• PM qualifications (e.g. PMP) and regulatory/cGMP knowledge would be a bonus.

Responsibilities

• Leading CMC projects from start to finish.
• Acting as the driving force between teams and external partners.
• Managing vendor relationships, budgets, timelines and risks.
• Supporting regulatory submissions and quality standards.

Skills

Project Management

Communication

Vendor Relationship Management

Problem Solving

Education

Degree in Life Sciences

Tools

Project Management Software

Job description

Overview

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.
• 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).

Qualifications

• 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.

Seniorities

• Mid-Senior level

Employment type

• Full-time

Job function

• Project Management

Industries

• Biotechnology Research, Pharmaceutical Manufacturing, and Research Services

Oxford, England, United Kingdom 4 days ago

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