Medical Director (Dermatology)

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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 clients 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. This role requires deep medical expertise to serve as the primary authority on medical issues, providing clear guidance and addressing complex questions related to medical, legal, and regulatory concerns.

Key Responsibilities

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

Qualifications (Max 5-6)

• Medical Qualifications: MD with specialist training and at least 5 years of clinical practice experience.
• 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: Ability to work effectively in fast-paced environments with shifting priorities and deadlines.
• Communication Skills: Excellent verbal and written communication skills, capable of conveying complex ideas clearly to diverse audiences.
• Professional Credibility: Trusted medical professional with a solid foundation in both clinical and research settings.

What We Offer

We offer a competitive compensation package, comprehensive benefits, and opportunities for personal and professional growth within a supportive 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 partner with biotechnology and pharmaceutical companies, providing tailored clinical development solutions. Our operations span 17 countries across Europe, North America, Asia Pacific, and the Middle East.

Our core values—Trust, Quality, Flexibility, and Passion—define our culture and work ethic and are integral to our success.