Director Clinical Development

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

Job summary

Une entreprise pharmaceutique basée au Royaume-Uni recherche un Directeur du Développement Clinique pour diriger des équipes et concevoir des essais cliniques dans le domaine des immunothérapies. Le candidat idéal aura une formation médicale, de l'expérience en recherche clinique et une forte capacité de collaboration internationale.

Qualifications

• GMC ou qualification équivalente.
• Expérience en tant que Principal Investigator dans des études avec médicaments expérimentaux.
• Minimum trois ans dans la recherche clinique et développement de médicaments.

Responsibilities

• Fournir un leadership médical et supervision des activités d'essai clinique.
• Évaluer régulièrement la sécurité et contribuer aux processus d'évaluation des risques.
• Soutenir la conception et l'exécution des plans de développement clinique.

Skills

Medical leadership

Clinical trial design

Risk evaluation

Collaboration

Education

Medical qualification

Advanced degree in medicine or scientific discipline

Job description

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Director Clinical Development, south west london

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Client:

ARTO

Location:

south west london, 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.