CK Group are recruiting for a Clinical Project Manager, to join a growing early-stage Biotechnology company based near Manchester on a permanent basis. This is a fantastic opportunity for an experienced Project Manager with a proven life science background in managing Phase I/II trials.
The Role
This is a key operational role, where you will be responsible for driving our clients oncology programme from final GLP tox through to a first‑in‑human Phase I trial. You will be the main point of contact and take ownership for coordinating CROs, stakeholders, vendors, and regulators to drive this exciting project to clinic.
Responsibilities
- Project leadership – build and maintain the integrated project plan for GLP tox, CMC, regulatory and clinical work‑streams.
- Compile and submit CTA/IND, ethics track RFIs, and manage agency correspondence (MHRA, FDA, EMA).
- Vendor & CRO management.
- Support protocol development, investigator brochure, and site selection.
- Stakeholder engagement and management.
Your Background
- Degree qualified/PhD (preferred) with working knowledge of oncology, liposomes or gene therapy.
- Proven and successful Project Manager with extensive experience coordinating or managing Phase I/II trials (CRO, biotech or NHS R&D).
- Experience with CTA or IND submission and tracking.
- Familiar with GxP, ICH, and MHRA processes.
Apply
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
Contact Details:
CK Group- Science, Clinical and Technical Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager in Ringway
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Some tips for your application 🫡
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