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Interim Director, Clinical Science

CK Group

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GBP 150 000 - 200 000
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Interim Director, Clinical Science
CK Group
Oxford
Hybride
GBP 150 000 - 200 000
Plein temps
Il y a 11 jours

Résumé du poste

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.

Prestations

Competitive day rate

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.

Responsabilités

  • 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.

Connaissances

Communication skills
Interpersonal skills
Team collaboration

Formation

Relevant PhD
Description du poste
Interim Director, Clinical Science

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.

Responsibilities
  • 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.
Qualifications
  • 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.
Benefits

Competitive day rate.

Apply

It is essential that applicants hold entitlement to work in the UK. Please quote job reference 155459 in all correspondence.

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