Senior / Medical Director (Dermatology) (m/f/d)

TN United Kingdom; London; On-site; GBP 80,000 - 120,000; Full time

Job summary

Join a leading global Contract Research Organization as a Senior Medical Director in Dermatology. This role involves overseeing medical safety and regulatory matters in clinical trials, providing expert guidance, and mentoring junior staff. Ideal candidates will have an MD and extensive experience in clinical research and regulatory compliance.

Benefits

Competitive compensation package

Comprehensive benefits

Opportunities for personal and professional growth

Qualifications

• At least 5 years’ experience in clinical practice.
• Strong understanding of GCP, ICH guidelines, and pharmacovigilance legislation.

Responsibilities

• Provide advanced medical input on study design and trial protocols.
• Conduct senior-level medical reviews of safety data and regulatory documents.
• Mentor junior medical staff and engage with clients.

Skills

Communication Skills

Adaptability

Professional Credibility

Education

Medical Doctor (MD)

Job description

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Senior / Medical Director (Dermatology) (m/f/d), London

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Client:

TFS HealthScience

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

89fd344368b0

Job Views:

3

Posted:

21.05.2025

Expiry Date:

05.07.2025

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Job Description:

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions.

Join Our Team as a Medical Director

About this role

As part of our Dermatology team, you will work alongside passionate and innovative professionals to help our customers achieve their goals.

The Senior Medical Director is a key member of the Project Delivery team, managing safety and medical matters independently in accordance with company policies, SOPs, and regulatory requirements. With deep medical expertise, this role serves as the primary authority on medical issues—providing clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns.

Key Responsibilities

• Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures.
• Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective.
• Regulatory & Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans.
• Medical Monitoring & Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation.
• Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation.
• Team & Client Engagement: Mentor junior medical staff, support SOP/tool development, and participate in client meetings and presentations.

Qualifications

• Medical Qualifications: Medical Doctor (MD) with specialist medical training and at least 5 years’ experience in clinical practice.
• Clinical Trial Expertise: Experience serving on safety data review boards or similar roles in clinical research.
• Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs.
• Adaptability: Comfortable working in fast-paced environments with shifting priorities and deadlines.
• Communication Skills: Excellent verbal and written communication skills, able to convey complex ideas clearly to diverse audiences.
• Professional Credibility: Trusted medical professional with a strong foundation in clinical and research settings.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and opportunities for personal and professional growth in a rewarding environment. Join a team that values collaboration, innovation, and making a difference in patients’ lives.

A Bit More About Us

Founded over 25 years ago in Lund, Sweden, we are a global CRO dedicated to ensuring patient safety and well-being. We offer tailored clinical development solutions to biotechnology and pharmaceutical companies and operate in 17 countries across Europe, North America, Asia Pacific, and the Middle East.

Our core values—Trust, Quality, Flexibility, and Passion—are the foundation of our culture and work ethic, guiding our organization and defining who we are.