European Medical Science Liaison
at Philips
71034 Böblingen, Baden-Württemberg, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Nov, 2024 | Not Specified | 11 Aug, 2024 | 3 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION
The European Medical Science Liaison will serve as an essential link between Philips Hospital Patient Monitoring’s Medical Office and healthcare professionals (HCPs) for the European Union. The role is responsible for establishing and maintaining credible relationships with key medical thought leaders, HCPs, and organizations. The role is to engage in fair, balanced, and objective scientific exchange with medical thought leaders; lead the organization of research consortia; support company and investigator-initiated studies; gather key insights to drive clinical and medical strategy; create evidence-based medical education content for external HCPs; and support clinical education to external healthcare providers. The role may include up to 70% travel.
Responsibilities:
- 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.
REQUIREMENT SUMMARY
Min:3.0Max:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
71034 Böblingen, Germany