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

Client : TFS HealthScience

Location : Rome

Job Category : Other

EU work permit required :

Job Reference : 2ee479189c62

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Posted : 31.05.2025

Expiry Date : 15.07.2025

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 (FSP) solutions.

Join Our Team as a Medical Director.

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, managing safety and medical matters independently in line with company policies, SOPs, and regulatory requirements. With deep medical expertise, this role serves as the primary authority on medical issues—providing guidance and answering complex questions related to medical, legal, and regulatory concerns.

• 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 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 medical insight into regulatory submissions and safety documentation.
• Team & Client Engagement : Mentor junior staff, support SOP/tool development, and participate in client meetings and presentations.

• Medical Doctor (MD) with specialist training in Dermatology and at least 5 years’ clinical practice experience.
• Experience in safety data review boards or similar roles in clinical research.
• Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and SOPs.
• Ability to work in fast-paced environments with shifting priorities.
• Excellent communication skills, both verbal and written.
• Trusted medical professional with a solid clinical and research background.

Competitive compensation, benefits, and opportunities for growth in a collaborative environment that values innovation and making a difference in patients’ lives.

Founded over 25 years ago in Lund, Sweden, we are a global CRO committed to patient safety. Operating in 17 countries across Europe, North America, Asia Pacific, and the Middle East, our core values are Trust, Quality, Flexibility, and Passion, which shape our culture and work ethic.