Interim Director, Clinical Science

Idibu; Oxford; Hybrid; GBP 150,000 - 200,000; Full time

Job summary

A well-funded Immunology biotech in Oxford is seeking a Director Clinical Science to lead clinical trials for Autoimmune treatments. The role requires extensive experience and a relevant PhD, focusing on trial design, biomarker strategies, and regulatory interactions. Competitive day rate offered, with hybrid work arrangements. Applicants must be entitled to work in the UK.

Benefits

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 and experience of working with Regulatory Authorities.

Responsibilities

• Play a lead role in the design execution and scientific management of clinical trials.
• Lead the development of biomarker strategy supporting clinical development endpoints.
• Contribute to the development and review of regulatory submissions.

Skills

Lead the development of clinical trial synopses

Strong communication and interpersonal skills

Experience in multi-disciplinary teams

Education

Relevant PhD

Job description

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.

Key duties will include

• 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 companys 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.

Job Details

Employment Type: Full Time

Experience: years

Vacancy: 1