Head of Research CV-Library Head of Research

Scienceabode; Manchester; On-site; GBP 70,000 - 100,000; Full time

Job summary

An innovative biotechnology firm near Manchester is seeking a Head of Research to lead their oncology program from GLP tox through to first-in-human clinical trials. This role requires a proven project manager with a strong background in life sciences, particularly in managing Phase I/II clinical trials. The ideal candidate will hold a PhD and possess expertise in oncology, with hands-on experience in drug development processes. Competitive salary and growth opportunities are offered in a dynamic early-stage environment.

Qualifications

• Degree qualified/PhD preferred, with working knowledge of oncology or gene therapy.
• Proven experience managing Phase I/II trials in CRO, biotech, or NHS R&D.
• Experience with CTA or IND submission and tracking.

Responsibilities

• Lead integrated project plan for GLP tox and clinical work-streams.
• Compile and submit CTA/IND, manage agency correspondence.
• Support protocol development and stakeholder engagement.

Skills

Project leadership

Vendor management

Stakeholder management

Knowledge of oncology

Familiarity with GxP and ICH processes

Education

PhD in a relevant field

Job description

CK Group are recruiting for a Head of Research to join a growing early‑stage Biotechnology company based near Manchester on a permanent basis. This is a fantastic opportunity for an experienced scientific leader with a proven life science background in early drug discovery and driving projects into First‑in‑Human / clinics.

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.

Salary: £70,000 – £100,000

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, manage agency correspondence (MHRA, FDA, EMA).
• Vendor & CRO management.
• Support protocol development, investigator brochure, 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 wealth of 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.

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.

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