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Interim Director, Clinical Science
Job summary
An established biotech company in Oxford is seeking an Interim Director of Clinical Science to lead clinical trials for Autoimmune treatments. The role requires a relevant PhD and extensive experience in early phase studies, particularly in Atopic Dermatitis or Psoriatic Arthritis. This hybrid role involves on-site work once a week and offers a competitive day rate.
Benefits
Qualifications
- Extensive experience of the design and oversight of early phase, small molecule Autoimmune studies.
- Experience of working with Atopic Dermatitis or Psoriatic Arthritis will be advantageous.
- In-depth knowledge of relevant regulatory requirements.
Responsibilities
- Play a lead role in the design, execution, and scientific management of clinical trials.
- Lead the development of clinical trial synopses and protocols.
- Contribute to the development and review of regulatory submissions.
Skills
Education
Salary: £700 - £800 per day
REF Number: v-155459
Consultant: Jim Gleeson
Contact: 01438 842973
Date Published: 29.09.2025
Industry: Biotech
Location: Oxford, Oxfordshire, England
Functional Expertise: Clinical Operations/Development, Research & Development
CK Group are looking for a Director, Clinical Science to join a well-funded Immunology biotech who are preparing for their lead candidate to start clinical trials.
This will be a hybrid role requiring you to be on-site in Oxford once a week, possibly less if you live further away.
- As Director, Clinical Science you will play a lead role in the design, execution and scientific management of clinical trials for a portfolio of Autoimmune treatments.
- Leading the development of clinical trial synopses, clinical protocols and other key clinical trial documents.
- Leading the development of biomarker strategy and implementation of plans to support early clinical development endpoints.
- Development of strong relationships with KOLs and investigational centres in order to facilitate strong scientific engagement with the company's clinical programs.
- Contribution to the development and review of regulatory submissions and interaction with Regulatory Authorities.
- Oversight of the review of study data in collaboration with biostatisticians and data scientists.
- A relevant PhD
- Extensive experience of the design and oversight of early phase, small molecule Autoimmune studies.
- Experience of working with Atopic Dermatitis or Psoriatic Arthritis will be advantageous
- An in-depth knowledge of relevant regulatory requirements and experience of working with Regulatory Authorities.
- Excellent communication and interpersonal skills, with the ability to work effectively in multi-disciplinary teams.
Competitive day rate.
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 155459 in all correspondence.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.
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