Contract Clinical Developer - Oncology

JR United Kingdom; London; Remote; GBP 80,000 - 120,000; Full time

Job summary

A leading biotech company near London is seeking a Contract Clinical Developer specializing in Oncology for a promising neuroblastoma trial. The successful candidate will lead global clinical trials, provide medical expertise, and collaborate with cross-functional teams. This role requires an MD and significant experience in clinical development, particularly in oncology, with a strong emphasis on leadership and communication skills.

Qualifications

• MD (or equivalent medical degree) required.
• Experience in neuroblastoma highly desirable.
• Strong experience in clinical development in the pharmaceutical or biotechnology industry.

Responsibilities

• Lead the execution and oversight of global clinical trials in high risk neuroblastoma.
• Collaborate with investigators and external partners to advance the clinical development program.
• Provide strategic medical input into trial design and regulatory submissions.

Skills

Clinical Development

Leadership

Communication

Collaboration

Scientific Acumen

Education

MD or equivalent medical degree

Board-certified in Oncology or Pediatric Oncology

Job description

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Contract Clinical Developer - Oncology, london

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Client:

RBW Consulting

Location:

london, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1

Posted:

23.05.2025

Expiry Date:

07.07.2025

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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.