Director Clinical Development

ARTO; Maidstone; Remote; GBP 70,000 - 100,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Clinical Development Physician to join their clinical team. This role involves providing medical leadership for clinical trials, conducting safety assessments, and collaborating with multidisciplinary teams. Candidates should have a medical qualification, experience in clinical research, and a background in immunology or respiratory diseases.

Qualifications

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

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.

Skills

Medical leadership

Clinical trial design

Risk evaluation

Collaboration

Education

Medical qualification with active registration

Advanced degree in medicine or scientific discipline

Job description

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Full Job Description

Location: United Kingdom, (Remote/Home office)

Contact:

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

They’re now looking to bring on a Clinicaldevelopment physician to support their clinical team, with experiencein independently medically monitoring supporting and clinical trialdesign. With the companies focus on immunotherapies for conditionswithin immunology, allergy and particularly within respiratory orimmune-mediated conditions, its an exciting role for a drivencandidate!!

Key Responsibilities

• Provide medical leadership and supervision for clinicaltrial activities.
• Conduct regular safety assessments andcontribute to risk evaluation processes.
• Support the designand execution of clinical development plans.
• Operateeffectively within a matrix-structured organization.
• Collaborate with multidisciplinary teams across regions andfunctions.

Qualifications

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