Responsibilities
- Act as a scientific expert for Medical Affairs within a defined region, engaging with external specialists and healthcare professionals to foster trust and scientific exchange.
- Serve as the primary medical contact for external experts, addressing their scientific inquiries and supporting appropriate understanding and use of company therapies.
- Design and implement scientific engagement strategies, contributing to cross-functional account planning when necessary.
- Classify and prioritize external experts according to established guidelines, ensuring accurate documentation of interactions and insights in internal systems.
- Strengthen the organization's scientific footprint in biologic therapy centers by supporting research, education, and scientific information requests.
- Enhance scientific knowledge across internal teams through presentations and updates, while preserving medical independence.
- Support the launch, monitoring, and follow-up of designated medical affairs studies and projects, including registries and post-authorization research.
- Collaborate with clinical development teams on interventional trials, including study initiation activities as part of broader R&D efforts.
- Coordinate with external investigators to manage proposals and requests for investigator-initiated research, linking them with appropriate medical teams.
- Participate in key scientific conferences, gather relevant data, and work with internal stakeholders to summarize findings that inform strategic decisions.
- Help physicians navigate requests for early access to treatments under compassionate use or named patient programs, in compliance with regulations.
- Provide scientific and technical support to key opinion leaders, external collaborators, and internal teams for the development of medical publications.
- Ensure all professional activities adhere to applicable laws, regulations, industry codes, company policies, and best practices.
Work Arrangement
On-site
