Medical Director / Senior Medical Director - Oncology

Precision for Medicine; Italia; Remoto; EUR 100.000 - 160.000; Tempo pieno

Descrizione del lavoro

A leading company in clinical research is seeking a Medical Director/Senior Medical Director specializing in Oncology to support development programs and ensure data integrity. The role requires extensive oncology experience and involves strategic engagement in clinical trials across various geographic regions.

Competenze

• 5+ years of clinical experience.
• 5+ years of experience in oncology clinical research.
• Ability for domestic and international travel (30% travel).

Mansioni

• Support Business Development by participating in RFP processes.
• Collaborate with Regulatory Affairs on drug development strategies.
• Assume responsibility for medical and safety monitoring on projects.

Conoscenze

Oncology clinical research

Clinical experience

Strategic analysis

Interpersonal skills

Presentation skills

Formazione

MD, DO, MBBS or equivalent medical qualifications

Board Certification in Oncology

Descrizione del lavoro

Precision for Medicine is hiring a Medical Director / Senior Medical Director - Oncology to join our team. Candidates can work remotely in any of the following locations : Italy, UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia.

Position Summary :

The Medical Director serves as the project physician and provides medical and scientific expertise to project teams. The Medical Director’s primary focus will be to ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety. This position also participates in the strategic planning and execution of critical development programs for a variety of clients in haematology and oncology, contributes to the development of Precision’s Medical team, and supports Business Development activities.

Essential functions of the job include but are not limited to :

• Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement.
• Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings.
• Write or edit scientific content of deliverables within budget and timelines.
• Collaborate with Regulatory Affairs on regulatory product landscape and strategies as part of overall drug development strategy.
• Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts).
• Review and revise protocols, case report forms, training materials, project-specific tools, analysis plans, study designs, clinical trial reports, and new drug applications.
• Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings, and figures as needed.
• Serve as a medical resource for study sites, the project team, and clients.
• Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions.
• Assume responsibility for medical and safety monitoring on assigned projects.
• Participate in feasibility discussions relating to specific project proposals.
• Develop training modules and provide training concentrating on disease states.
• Participate in process improvement activities.
• Collaborate with the Senior Vice President, Global Medical, and other members of the Medical Science Department to support growth and development activities globally.

Qualifications : Minimum Required :

• MD, DO, MBBS, or equivalent medical qualifications.
• 5+ years of clinical experience.
• 5+ years of experience in oncology clinical research.
• Board Certification in Oncology.
• Demonstrated expertise around the lifecycle of oncology drug development with the ability to strategically analyze oncology clinical trial protocols.
• Availability for domestic and international travel including overnight stays (approximate 30% travel requirement).

Preferred :

• Drug development experience in Oncology.
• Oncology Fellowship or equivalent.
• Phase I and Phase II oncology clinical trial experience.
• Prior CRO experience.
• Maintains current scientific and medical knowledge base.
• Ability to deliver on commitments; understands the service culture.
• Strategic thinker who can build strategic drug development solutions associated with novel development programs, study designs, and patient populations.
• Demonstrates a high degree of professionalism, as evidenced by punctuality and positive interactions with customers and teammates, including good interpersonal skills.
• Communicate both verbally and in written form in an acceptable manner.
• Conduct formal presentations to a wide variety of audiences including colleagues.
• Strong visual and presentation skills.
• Ability to work effectively in a fast-paced team setting, with minimal supervision.

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease.

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