Deputy Chief Medical Officer

LinkedIn; Roma; In loco; EUR 120.000 - 180.000; Tempo pieno

Descrizione del lavoro

Philogen seeks a Deputy Chief Medical Officer to lead medical oversight for clinical programs and trials. You will guide strategy, study design and regulatory submissions while coordinating with R&D and biostatistics teams to ensure safe, compliant product development.

The role requires a medical degree and substantial clinical trial experience, with influence across global regulatory standards and partner relations.

Competenze

• Educational Requirements: A degree in Medicine (mandatory requirement)

Mansioni

• Provide medical oversight and leadership to ensure strategy, development and implementation of clinical trials.
• Support the R&D department in planning product availability for clinical studies.
• Supervise pharmacovigilance, monitor patient safety and ensure global regulatory standards.
• Interpret emerging study data to guide development strategies.
• Coordinate discussions with health authorities, regulatory teams and clinical centers; build relationships with leading physicians.
• Coordinate Medical and Biostatistics teams.

Conoscenze

Medical Doctor

Formazione

Medical degree

Descrizione del lavoro

Deputy Chief Medical Officer

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About us

Philogen is a Swiss–Italian integrated biotechnology company founded in 1996, focused on the development of innovative biopharmaceuticals for cancer therapy and inflammatory diseases ().

Philogen discovery center is located in Otelfingen (Zurich, Switzerland). Preclinical candidates developed at Philochem are subsequently manufactured at Philogen's authorized GMP facilities in Siena (Italy).

Philogen currently sponsors and coordinates Phase I, II, and III clinical trials in Europe and the United States. The clinical department is based in the Siena, Milan, and Zurich offices.

Your Role

We are seeking a highly motivated and collaborative Medical Doctor to join as Deputy Chief Medical Officer.

You will play a key role in providing medical oversight , expertise and leadership to ensure the strategy, development and implementation of clinical trials, supporting the R&D; department in planning product availability for clinical studies.

Key Responsibilities

• Provide support in developing strategic plans for the company's product portfolio to ensure development programs.
• Support the design of study protocols, medical reports, statistical analysis plans and regulatory application documentation
• Supervise pharmacovigilance, monitoring patient safety and ensure global regulatory standards
• Interpret emerging study data to guide development strategies.
• Interact with regulatory and project management teams to coordinate discussions with health authorities and clinical centers and develop relations with leading physicians.
• Appropriately represent Philogen when building and maintaining relationships with partners.
• Coordinate Medical and Biostatistic teams.

Who We Are Looking For

• Educational Requirements: A degree in Medicine (mandatory requirement)
• Required Experien