Contract Clinical Developer - Oncology

JR United Kingdom; Slough; Remote; GBP 80,000 - 110,000; Full time

Job summary

A leading biotech company near London seeks a Contract Clinical Developer specializing in oncology and neuroblastoma. In this role, you will lead global clinical trials and collaborate with multidisciplinary teams, contributing to the advancement of innovative therapies. Ideal candidates will possess an MD, board certification, and significant clinical development experience.

Qualifications

• MD required, Board-certified in Oncology preferred.
• Experience in neuroblastoma highly desired.
• Proven track record leading global clinical trials.

Responsibilities

• Lead execution and oversight of global clinical trials.
• Provide strategic medical input into trial design and regulatory submissions.
• Collaborate with investigators and external partners.

Skills

Clinical development experience

Strong scientific acumen

Excellent communication skills

Leadership skills

Education

MD or equivalent medical degree

Board-certified in Oncology or Pediatric Oncology

Job description

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Contract Clinical Developer - Oncology, slough

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Client:

RBW Consulting

Location:

slough, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

A Director of Clinical Development is required to drive clinical development in a very promising trial for neuroblastoma. You will be working on a remote basis with a fast rising biotech company which has recently received a large amount in investment funding to move their ambitious program forward. They are based near London.

Job role

• Participate as a key component in setting the development strategy in high risk neuroblastoma
• Lead the execution, and oversight of global clinical trials in high risk neuroblastoma.
• Serve as clinical lead on cross-functional project teams including regulatory, clinical operations, medical affairs, and commercial colleagues.
• Provide strategic medical input into trial design, protocol development, and regulatory submissions.
• Collaborate with investigators, KOLs, and external partners to advance the clinical development program.
• Provide medical expertise and guidance to internal teams throughout the drug development lifecycle.

Requirements

• MD (or equivalent medical degree) is required.
• Board-certified (or eligible) in Oncology or Pediatric Oncology is highly preferred.
• Experience in neuroblastoma is highly desirable.
• Strong experience of clinical development experience in the pharmaceutical or biotechnology industry.
• Proven track record in leading global clinical trials and working with regulatory authorities (FDA, EMA).
• Strong scientific acumen, clinical judgment, and ability to interpret and communicate clinical data.
• Willingness and ability to travel 50–60% internationally (EU and US).
• Excellent communication, collaboration, and leadership skills.

For more information on this role and the high profile biotech you will be working with please CLICK APPLY and forward your CV.