Director Clinical Development

JR United Kingdom; West Midlands Combined Authority; Remote; GBP 80,000 - 120,000; Full time

Job summary

A leading UK-based Pharma is seeking a Director of Clinical Development to guide their clinical team in launching innovative immunotherapies. The role involves medical leadership in clinical trial activities, risk evaluations, and collaboration with cross-functional teams, ideal for a candidate with a strong background in clinical research.

Qualifications

• Experience as a Principal Investigator in Phase 1 trials.
• At least three years in clinical research and drug development.
• Background in respiratory or immunological conditions is advantageous.

Responsibilities

• Provide medical leadership for clinical trial activities.
• Conduct safety assessments and risk evaluations.
• Support clinical development plans design and execution.

Skills

Medical leadership

Clinical trial design

Safety assessments

Risk evaluation

Collaboration

Education

Medical qualification with active registration

Advanced degree in medicine or scientific discipline

Job description

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Director Clinical Development, west midlands

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Client:

ARTO

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Location: United Kingdom, (Remote/Home office)

ARTO is partnered with UK based Pharma looking to expand their early-stage pipeline and preparing for upcoming clinical trials across Europe and the US.

They’re now looking to bring on a Clinical development physician to support their clinical team, with experience in independently medically monitoring supporting and clinical trial design. With the companies focus on immunotherapies for conditions within immunology, allergy and particularly within respiratory or immune-mediated conditions, its an exciting role for a driven candidate!!

Key Responsibilities

• Provide medical leadership and supervision for clinical trial activities.
• Conduct regular safety assessments and contribute to risk evaluation processes.
• Support the design and execution of clinical development plans.
• Operate effectively within a matrix-structured organization.
• Collaborate with multidisciplinary teams across regions and functions.

Qualifications

• Medical qualification with active registration (e.g., GMC or equivalent).
• Previous role as a Principal Investigator in studies involving investigational drugs, ideally with early-phase (Phase 1) human trials experience.
• At least three years working within clinical research and drug development.
• Background in respiratory diseases or immunological conditions is advantageous.
• Proven track record of facilitating cross-regional team meetings (including UK, EU, and US-based collaborators).
• An advanced degree in medicine or a scientific discipline (MD, PhD, or equivalent) is preferred.
• Additional certification in Pharmaceutical Medicine or progress toward a CCT in the field is seen as a strong asset.