Regional Medical Director Italy, Greece, Turkey, E Europe – Immuno-oncology

Regional Medical Director – Italy, Greece, Turkey, E Europe – Immuno-oncology

IQVIA are delighted to be partnering with a customer passionate about immuno-oncology who are working on therapies that can harness the power of the body’s immune system to both treat and potentially cure cancer. We are seeking an experienced Regional Medical Director to work in a dynamic and collaborative environment and to be responsible for clinical and strategic leadership of the regions medical affairs activities including launch readiness support, launch, and refinement / execution of Phase 3 and post approval studies.

Role and responsibilities

• Provide clinical & scientific leadership for the company’s oncology products and pipeline
• Support the development of complex clinical data through clinical trials, real world evidence generation and investigator sponsored studies.
• Responsible for leading insight gathering by regularly communicate with the external medical community to generate insights and inform product strategy via advisory boards strategic insight gathering and landscape assessment
• Provide input and guidance to the medical information and professional strategies teams within their region
• Ensure compliance with regional directives of, amongst others, release of promotional material, medical representative training materials and medical information
• Work closely with Medical Science Liaisons (MSLs) on training and scientific communication to ensure successful execution of tactics in support of medical strategy
• Serve as subject matter expert in the disease areas of interest
• Act in accordance with company policies and utilize best practices, including, for example, the Code of Business Conduct, ethics and Standards of General Data Protection regulations (GDPR).
• Support the development of a robust publication, congress, and Key Opinion Leader (KOL) strategies
• Monitor local and regional pharmacovigilance requirements and maintenance of local legislation repository in collaboration with Global Safety Operations.

Qualifications and Experience

• MD, PharmD, DO, or PhD (with relevant clinical experience)
• Seven years of medical affairs strategy or medical director role
• Solid tumor oncology therapeutic experience
• Prior medical affairs experience and product life cycle management experience
• Experience and understanding of drug development in oncology
• Industry experience in medical affairs / clinical development at a biotech or pharma
• Ability to travel.

So, if you’re looking for an inspiring environment with passionate colleagues, and a culture that nurtures learning, innovation and team success, we invite you apply.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity, and intellectual courage every step of the way. Learn more at jobs.iqvia.com .

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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