Director Clinical Development

JR United Kingdom; Kingston upon Hull; Remote; GBP 80,000 - 110,000; Full time

Job summary

A leading pharmaceutical company is seeking a Director of Clinical Development to enhance their pipeline for immunotherapy treatments. The role focuses on medical leadership, monitoring, and oversight of clinical trials, ideal for candidates with significant experience in clinical research and a strong medical background.

Qualifications

• Minimum three years in clinical research and drug development.
• Experience as a Principal Investigator in early-phase clinical trials preferred.
• Background in respiratory diseases or immunological conditions advantageous.

Responsibilities

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

Skills

Medical leadership

Clinical trial design

Cross-regional collaboration

Education

Medical qualification with active registration

Advanced degree in medicine or scientific discipline (MD, PhD)

Job description

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Director Clinical Development, kingston upon hull, east yorkshire

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Client:

ARTO

Location:

kingston upon hull, east yorkshire, United Kingdom

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.