In this role you will provide medical leadership for clinical trials, guiding scientific strategy, trial execution, and reporting. You will serve as the internal medical expert for study results interpretation and contribute to protocol and project design. You will collaborate with cross-functional teams to manage safety, regulatory documents, and manuscripts, and participate in business development as needed. The position offers hybrid work flexibility and opportunities to influence trial design and medical strategy within a biotech/pharma CRO environment. This role appeals to a physician who wants to shape clinical programs and drive meaningful therapeutic work.

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Provide medical management and expertise for clinical trials

Contribute medical input to study reports, regulatory documents, and manuscripts





Manage safety issues in clinical trials in collaboration with the team

Participate in business development through proposal and sponsor meetings

Coordinate with other departments across feasibility, design, medical information, and document review/editing

Lead adherence to research protocols and policies

Influence study planning, protocol development, and project plans

MD degree or equivalent

Board certification and current medical licensure preferred

Prior clinical trial research experience preferredPrevious experience in pharmaceutical-related clinical research preferred

collaboration and cross-functional teamwork

clear scientific communication

problem-solving and risk assessment

clinical trial management

study design and protocol development

regulatory document preparation and review

Dermatologist - Medical Director varese, lombardia, it

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📌 Dermatologist - Medical Director (Varese)
🏢 Altro
📍 Varese