Director Clinical Development

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

Job summary

A leading UK-based pharma company is seeking a Clinical Development Physician to provide medical leadership for clinical trials focused on immunotherapies. The ideal candidate will have experience in medical monitoring, trial design, and substantial clinical research experience. This remote position offers an exciting opportunity to contribute to groundbreaking therapies.

Qualifications

• At least three years of experience in clinical research and drug development.
• Experience as a Principal Investigator in Phase 1 trials.
• Background in respiratory or immunological conditions is advantageous.

Responsibilities

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

Skills

Medical monitoring

Clinical trial design

Safety assessments

Collaboration

Education

Medical qualification with active registration

Advanced degree in medicine or scientific discipline

Certification in Pharmaceutical Medicine

Job description

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Director Clinical Development, Colchester

Client:

ARTO

Location:

Colchester, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

2

Posted:

31.05.2025

Expiry Date:

15.07.2025

Job Description:

Location: United Kingdom, (Remote/Home office)

ARTO is partnered with a UK-based pharma company looking to expand their early-stage pipeline and prepare for upcoming clinical trials across Europe and the US.

They are seeking a Clinical Development Physician to support their clinical team, with experience in medical monitoring and clinical trial design. The company's focus is on immunotherapies for conditions within immunology, allergy, and respiratory or immune-mediated conditions. This is an exciting opportunity for a driven candidate!

Key Responsibilities

• Provide medical leadership and supervision for clinical trial activities.
• Conduct safety assessments and contribute to risk evaluations.
• Support the design and execution of clinical development plans.
• Work 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).
• Experience as a Principal Investigator in studies involving investigational drugs, ideally with early-phase (Phase 1) trials.
• At least three years of experience in clinical research and drug development.
• Background in respiratory or immunological conditions is advantageous.
• Experience facilitating cross-regional team meetings (UK, EU, US).
• Advanced degree in medicine or a scientific discipline (MD, PhD, or equivalent) preferred.
• Additional certification in Pharmaceutical Medicine or progress toward a CCT is a strong asset.