Clinical Project Manager

CK Group- Science, Clinical and Technical; Ringway; On-site; GBP 60,000 - 80,000; Full time

Job summary

A growing biotechnology company based near Manchester is seeking a Clinical Project Manager to drive an oncology program from GLP tox to first-in-human Phase I trials. The ideal candidate has a proven track record in managing Phase I/II trials, a relevant degree, and familiarity with regulatory processes. This permanent role offers a key opportunity to lead and coordinate projects in the life sciences sector.

Qualifications

• Experience coordinating or managing Phase I/II trials.
• Knowledge of oncology, liposomes, or gene therapy.
• Familiarity with GxP, ICH, and MHRA processes.

Responsibilities

• Lead project plan for GLP tox, CMC, regulatory and clinical workstreams.
• Compile and submit CTA/IND, ethics track RFIs.
• Manage agency correspondence (MHRA, FDA, EMA).
• Support protocol development and site selection.

Skills

Project leadership

Vendor & CRO management

Stakeholder engagement

Regulatory submission knowledge

Education

Degree in life sciences or PhD (preferred)

Job description

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.