Interim Director, Clinical Science

CK Group- Science, Clinical and Technical; Oxford; Hybrid; GBP 150,000 - 200,000; Full time

Job summary

A leading Immunology biotech based in Oxford is seeking a Director, Clinical Science to lead the design and management of clinical trials for autoimmune treatments. This hybrid role offers a competitive day rate and requires extensive experience in clinical trial oversight, strong communication skills, and a relevant PhD. You will be responsible for developing clinical trial documents, biomarker strategies, and engaging with regulatory authorities.

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.

Responsibilities

• Lead role in design and execution of clinical trials.
• Develop clinical trial synopses, protocols, and key documents.
• Develop biomarker strategy for early clinical development.
• Build relationships with KOLs and investigational centers.
• Contribute to regulatory submissions and interact with authorities.
• Review study data with biostatisticians and data scientists.

Skills

Clinical trial design

Regulatory requirements knowledge

Communication skills

Interpersonal skills

Education

PhD in a relevant field

Job description

Overview

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 (phone number removed) in all correspondence