Director Clinical Development

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

Job summary

Une entreprise pharmaceutique britannique cherche un Directeur en Développement Clinique pour soutenir leurs essais cliniques dans le domaine des immunothérapies. Le candidat idéal doit avoir une expérience significative dans le suivi médical, la planification d'essais cliniques et travailler au sein d'équipes multidisciplinaires. Ce rôle offre une belle opportunité de contribuer à des avancées dans le traitement des conditions respiratoires et immunologiques.

Qualifications

• Qualification médicale et enregistrement actif requis (GMC ou équivalent).
• Expérience en tant qu'enquêteur principal dans des études humanitaires, idéalement en Phase 1.
• Au moins trois ans dans la recherche clinique et le développement de médicaments.

Responsibilities

• Fournir leadership et supervision pour les activités des essais cliniques.
• Effectuer des évaluations de sécurité et contribuer à l'évaluation des risques.
• Collaborer avec des équipes multidisciplinaires à l'échelle internationale.

Skills

Leadership médical

Évaluation des risques

Planification clinique

Collaboration multidisciplinaire

Education

Qualification médicale avec enregistrement actif

Diplôme avancé en médecine ou discipline scientifique

Job description

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Director Clinical Development, warrington, cheshire

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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.