About the RoleKey Responsibilities: Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish response documents for frequently asked questions.Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the respective therapeutic area.Support country strategy for Non-Interventional Studies/Investigator Initiated Trial activities.Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for partner engagement and events are tailored to local needs and reviewed/approved per local/P3 guidelines.Ensure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of internal controls within the area of responsibilities.Minimum Qualifications: University degree in life science is mandatory, physician (MD) is desirable.Validated experience in similar roles.Deep understanding of national Healthcare System.Cross-functional collaboration.Strategic mindset / agile learning.Availability to do up to 30% of field work.Commitment to Diversity and Inclusion
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Combining to achieve breakthroughs that change patients' lives.
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Functional Area: Research & Development
Job Type: Full time
Employment Type: Regular
Shift Work: No
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