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Establishes, maintains, and cultivates credible relationships with key medical thought leaders, HCPs, and scientific professionals.
Participates in medical congresses by attending scientific sessions, meeting with key thought leaders, and gathering insights for consolidation and dissemination to internal cross functional teams.
Drive the development of research consortia in alignment with Hospital Patient Monitoring’s research strategy in Europe.
Collaborates with Medical Affairs and Clinical Development teams to support the development and execution of company sponsored clinical studies.
Contributes to investigator-initiated studies (IIS), including conducting study feasibility assessments and collaborating with investigators to facilitate clinical research.
Facilitate the intake and prioritization of collaborative research requests from potential investigators
Supports the management of medical advisory boards including selection of advisors, content development, and overall strategic planning.
Develops and delivers credible scientific presentations on the company’s products as well as related published literature ensuring stakeholders have a clear understanding of how the company’s evidence fits within clinical practice.
Develops medical education material, such as white papers, for external use.
Collaborates with key customers and institutions to realize testimonials.
Assist cross-functional teams in literature reviews to answer relevant clinical and medical questions.
Support the promotional review committee as the medical reviewer, as needed
Responds to on and off-label questions from HCPs, providing accurate and balanced scientific responses to build trust and credibility.
Works under general supervision and adheres to organizational policies, industry regulations, and ethical standards in all interactions and activities, ensuring ethical conduct and integrity in scientific engagements.
The role may include up to 70% travel in Europe and seldomly travel to the US as needed for team meetings.
Have education in: Advanced Clinical/ Science Degree such as PharmD, MD, PhD, DNP or equivalent. (It’s highly preferred that you have a doctorate level degree (PhD, PharmD, DNP, MD).) It’s preferred that you have an established history of publications.
Have the following experience:
Doctorate level degree and
5+ years of experience as a medical science liaison,
2+ years organizing research consortia from a medical device or pharmaceutical industry perspective,
3+ years of experience of in-patient acute care clinical practice, preferably in critical care or perioperative medicine, or 5+ years of experience in clinical research related to the therapeutic area
Possess significant skills in both verbal and written communication to collaborate with and influence cross-functional teams such as Clinical Affairs, Product Management, R&D, and Clinical Marketing.
The ideal candidate has experience working in the hospital as well as experience within the Medical Affairs department of either a medical device or pharmaceutical company, particularly as a Medical Science Liaison.
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