Medical Director

CK Group- Science, Clinical and Technical; Cambridge; On-site; GBP 200,000 +; Full time

Job summary

A leading consultancy in healthcare is seeking a Medical Director in Cambridge. You will advise on clinical development strategies, lead medical input on projects, and act as an independent physician. Ideal candidates will possess a medical degree and substantial drug development experience, particularly in consultative roles. This position offers a competitive salary and excellent benefits.

Benefits

Excellent benefits package

Qualifications

• Substantial experience in drug development ideally within a consultancy or advisory capacity.
• Expertise in developing and operationalizing clinical development plans.
• Medical input into regulatory strategies and processes.

Responsibilities

• Advise clients on clinical development strategies and medical governance.
• Lead strategic input to client projects and documents.
• Act as an independent physician and medical monitor for studies.

Skills

Clinical development strategies

Medical governance frameworks

Regulatory pathways

Safety monitoring

Medical affairs strategy

Education

Medical Degree (MBBS, MBChB, MD) and GMC registration

Post-graduate qualifications and Diploma in Pharmaceutical Medicine

Job description

Overview

CK Group are recruiting for a Medical Director to join a highly respected consultancy working with clients on a global basis to help develop and commercialise new medicines.

Responsibilities

• Advise clients on clinical development strategies, medical governance frameworks, and global regulatory pathways.
• Lead strategic medical input to client projects and documents as required, e.g., project budgets, clinical development plans, target product profiles and due diligence support.
• Review and provide input into essential documents, e.g., IB, protocols, PIS/ICF, SAP, Safety/PVMPs, DMPs, CRFs and CSR.
• Act as an independent physician and medical monitor for an assigned study on behalf of the client, as per the ICH Guideline for Good Clinical Practice E6 (R2).
• Guide medical affairs teams in scientific communications. Advise on medical affairs strategy including KOL engagement, publication planning, and scientific communications.
• Contribute medical expertise by acting as the trial level physician and medical monitor to facilitate the set-up, execution, analysis and reporting the results of clinical trials in line with current regulatory and ethical guidelines.
• Maintain oversight of patient safety and safety monitoring in the assigned study, participate in Safety Review/DSMBs as required, and be a designated point of contact for the site team and sponsor on any safety-related matters as outlined in the MM and Safety Plans.

Your Background

• A Medical Degree (MBBS, MBChB, MD) and GMC registration, preferably with post graduate qualifications and Diploma in Pharmaceutical Medicine.
• Substantial experience in drug development ideally within a consultancy or advisory capacity.
• Expertise in developing and operationalizing clinical, designing clinical development plans. Medical input into regulatory strategies and processes, such as IND NDA and MAAs.

Salary

Competitive with an excellent benefits package

Apply

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.

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