Associate Director, Global Medical Affairs Training - Plainsboro Township

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. · Work with the Medical Affairs Program Development & Training directors to streamline therapeutic resources, support onboarding curr ...

The Medical Affairs Training & Resources intern will work with the Medical Affairs Program Development & Training directors to streamline therapeutic resources, support onboarding curricula, ensure resources provide strategic communication points, expand utilization of learning s ...

About The Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. · ...

The Associate Director, Global Medical Affairs Training is responsible for developing implementing continuously elevating Genmab training curricula supporting Health Evidence Outcomes Liaisons HEOLs cross-functional Medical Affairs partners. · Strategic Training Leadership Provid ...

At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion ...

About The Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to pr ...

The Medical Promotional Review Specialist ensures the scientific accuracy, clinical appropriateness, and regulatory validity of promotional materials from a medical and scientific perspective. · Demonstrated expertise in reviewing medical literature and evaluating scientific vali ...

This role involves analyzing and summarizing data to create responses to unsolicited medical information inquiries. · ...

Analyzes and summarizes available data and creates / authors responses to unsolicited inquiries from healthcare professionals, institutions, and/or payors requesting medical information about Novo Nordisk products. · ...

+Job summary · A Medical Information Specialist analyzes and summarizes available data and creates responses to unsolicited inquiries from healthcare professionals. · +Provides verbal, written, and on-demand video responses to unsolicited medical and technical inquiries about Nov ...

The Medical Promotional Review Specialist ensures scientific accuracy and clinical appropriateness of promotional materials from a medical/scientific standpoint. · ...

Ensure scientific accuracy and clinical appropriateness of promotional materials from a medical/scientific standpoint. · Serve as a member of the Promotional Review Board (PRB).PharmD / MD/ DO / NP with a minimum of two years of relevant professional experience. · Thorough unders ...

The Senior Medical Information Specialist will analyze and summarize available data, create responses to unsolicited inquiries from healthcare professionals, institutions, and/or payors requesting medical information about Client's products. · ...

Analyze and summarize available data and create responses to unsolicited inquiries from healthcare professionals. · Med Info experience · Clinical experience is a plus if no Medical Info experience · ...

The Director is Responsible for leading the Program Management and FRM teams and supports strategies that maximize access to therapies. Are you ready to realize your potential? · This individual will maintain a high-level of collaboration and integration with all relative field t ...

The Director is Responsible for leading the Program Management and FRM teams and supports strategies that maximize access to therapies. · ...

The Director is responsible for leading the Program Management and FRM teams and supports strategies that maximize access to therapies. · Develops Field Reimbursement strategy and partners across PSS team to develop materials and educate FRM teams on program solutions. · Provide ...

Senior Medical Affairs Operations System Owner Manager · Facility: Project Management & Agile · Location:Plainsboro, NJ, US · About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within th ...

We're not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. · ...

+Responsible for providing legal support to the Clinical Development, Medical & Regulatory Affairs (CMR) organization at Novo Nordisk Inc. · +Provide high-quality legal support relating to Novo Nordisk research and development activities. · Draft, negotiate and review a broad set ...