Director Clinical Development

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

Job summary

Une société pharmaceutique basée au Royaume-Uni recherche un Directeur du Développement Clinique pour diriger des activités d'essais cliniques, en se concentrant sur l'immunothérapie pour les conditions respiratoires et immunologiques. Le candidat idéal aura un parcours significatif en recherche clinique, avec des antécédents de supervision d'études aux phases précoces.

Qualifications

• Expérience en tant qu'investigateur principal dans des études avec médicaments expérimentaux.
• Minimum de trois ans d'expérience en recherche clinique et développement de médicaments.
• Antécédents en maladies respiratoires ou conditions immunologiques sont avantageux.

Responsibilities

• Fournir leadership médical et supervision pour les activités d'essais cliniques.
• Effectuer des évaluations de sécurité et contribuer aux processus d'évaluation des risques.
• Soutenir la conception et l'exécution des plans de développement clinique.

Skills

Leadership médical

Supervision d'essais cliniques

Collaboration multidisciplinaire

Education

Qualification médicale avec enregistrement actif (ex. GMC)

Diplôme avancé en médecine ou discipline scientifique (MD, PhD)

Job description

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Director Clinical Development, birmingham

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Client:

ARTO

Location:

birmingham, 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.