Medical Director (Dermatology)

TN United Kingdom; London; On-site; GBP 90,000 - 150,000; Full time

Job summary

Join a forward-thinking organization as a Medical Director, where your expertise will shape the future of clinical trials in dermatology. You will be part of a dynamic team, guiding safety and medical matters while ensuring compliance with regulatory standards. This role offers the chance to mentor junior staff and engage with clients, making a real impact on patient safety and well-being. Enjoy a competitive compensation package and the opportunity for personal and professional growth in a collaborative environment that values innovation and quality.

Benefits

Comprehensive benefits

Competitive compensation package

Personal and professional growth opportunities

Qualifications

• 5+ years of clinical practice experience as a Medical Doctor.
• Strong understanding of GCP and ICH guidelines.

Responsibilities

• Provide advanced medical input on study design and trial protocols.
• Mentor junior medical staff and support SOP/tool development.

Skills

Medical Doctor (MD)

Clinical Trial Expertise

Regulatory Knowledge

Communication Skills

Adaptability

Education

Medical Degree

Job description

Social network you want to login/join with:

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire 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 ensure our customers achieve their goals.

The Senior Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (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 join Commercial Operations in client meetings and presentations.

Qualifications (Max 5-6)

• 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 equivalent 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, able to convey complex ideas clearly to diverse audiences.
• Professional Credibility: Trusted medical professional with a strong foundation in both clinical and research settings.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 25 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific, and the Middle East.

Our core values of Trust, Quality, Flexibility, and Passion are what make TFS HealthScience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.