Field Medical Advisor - Italy

Please, note that we will consider candidates based only in Center/South Italy.

This is a fixed term contract (1 year) with the possibility to be extended/become permanent.

You are a listener, an educator and a gifted cultivator of new and exciting opportunities grounded in science?

The Field Medical Advisor (FMA) serves as the primary field-based point of contact with Key Opinion Leaders (KOLs), Healthcare Providers (HCPs) including clinical investigators on a range of clinical and scientific issues.

The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client.

This includes the provision of scientific and medical data on both licensed and unlicensed client products and indications as permissible by local laws and regulations.

The FMA identifies, develops, and maintains long-term collaborative partnerships with external clinical and scientific experts and institutions to provide support for current and future client portfolio activities.

They will ensure effective communication and collaboration across a multifunctional client team including other Medical Affairs colleagues as well as commercial and Market Access to meet client and healthcare provider needs and ultimately ensure the best patient care in an efficient and compliant manner.

Responsibilities

• Develops and maintains in a self-driven manner outstanding knowledge of relevant disease area topics
• Develops and maintains in a self-driven manner outstanding knowledge of client products, competitor products, and other therapeutic options within the therapeutic area
• Collaborates with the cross functional team to ensure the best patient care
• Maintains an in-depth understanding of the medical strategy and broader client strategy to ensure their own activities are coordinated with the team and aligned to the clients strategy
• Collaborates with Cluster (and Country Medical Leads) for the development and execution of the field medical strategy for the product and disease area
• Maintains and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities
• Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws
• Engages with cross-functional team to ensure (their own) activities are coordinated with the team and aligned to client strategy
• Initiates and leads the implementation of medical projects, e. g. Medical Advisory Board meetings, Medical Education, (patient) care innovation projects
• Provides scientific congresses coverage and support (national and international) client planned activities
• Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings
• Responds to unsolicited requests for medical information on client products in a credible, balanced/objective manner
• Proactively engages with HCP community to provide medical education as permissible by local laws and regulations
• Provides effective clinical presentations to internal and external audiences and tailors presentations to meet specific audience needs
• Supports Early Access Programmes (EAPs)
• Identifies and maps HCPs and networks/referral patterns
• Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners
• Support clinical operations in trial site identification
• Facilitate clear communication between the client and investigators in investigator engagement for both client sponsored and investigator-sponsored studies and address barriers to enrolment for pipeline assets
• Identify and support local data generation activities

Requirements

• MSL/FMA experience
• Advanced degree (MD, Ph D, Pharm D) or professionally qualified (physician, nurse pharmacist). Exceptional candidates with MSc considered.
• experience within disease area (as part of academia or in industry)
• Knowledge of clinical research design and GCP in the disease area.
• Demonstrates strong understanding of clinical research trial design and study analysis including cost effectiveness and other high-level HEOR evidence approaches
• Demonstrates strong understanding of local healthcare systems, treatment guidelines
• Demonstrate ability to develop trust and maintain integrity with KOLs/External Clinical and Scientific Experts, investigators, HCPs, and institutions, as well as with peers, and others.
• Demonstrate knowledge of relevant laws and regulations to role
• Excellent presentation, communication skills
• Ability to convey complex scientific concepts and information appropriately tailored to the audience e. g., affiliate staff and regional / global Medical Affairs leadership

Syneos Health is an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against.

If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at: Email: [email protected]

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