- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) Immunology/Pipeline & Biomarkers will be responsible for driving execution of ... medical affairs experience (eg, Regional Director Medical Affairs ) with proven...or SLE or SSc Vitiligo and understanding of the US market)Strong prioritization and decision-making skillsAbility to effectively collaborate… more
- Lundbeck (Chicago, IL)
- …candidates anywhere in the Greater United StatesSUMMARY:The Sr. Dir. Medical Affairs Future Product Portfolio will secure US medical insights for ... especially Digital & Data Analytics function, to accelerate needed infrastructure within US Medical Affairs . We seek a senior, strategic and highly adaptable… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Board meetings for a Therapeutic Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior Medical ... development, CMR is involved. The one thing that keeps us all marching to the same beat is our...portfolio. Relationships This position reports directly to the Executive Director , Medical Affairs and will… more
- Novo Nordisk Inc. (Chicago, IL)
- …of TA priorities and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...for scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial… more
- Eisai, Inc (Nutley, NJ)
- …to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics for ... assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible...the employment eligibility of all new hires in the United States . Please click on the following… more
- Merck & Co. (North Wales, PA)
- …of Physician Editor at the Manuals. This is an opportunity to use your medical knowledge and editorial skills to contribute to medical education and clinical ... 400 leading academic external authors and editors to provide high quality medical information to professionals and patients. The Manuals, a trusted resource since… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... into the Oncology drug development preferred.Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... review and approval of all US promotional materials and serving as the promotional regulatory...as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex- ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... trial protocol development and reviews (clinical trial protocols and medical device protocols)ICF reviews to ensure adequate disclosure for collection,… more
- Merck & Co. (North Wales, PA)
- …the Director may be responsible for: Providing scientific and medical leadership for strategic alliances and Co-partnership opportunities.-Supporting the team in ... - one that is ready to help create a healthier future for all of us . Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and… more
- Merck & Co. (North Wales, PA)
- …is a member of several cross-functional teams, including the Promotional Review Team (PRT), and the US and Global Medical Affairs Teams. In PRT, the MCRP is ... with physicians to answer MIRs.-Proactively engage with leaders and participate in US and Global Medical Affairs Teams to ensure that sufficient medical … more
- Merck & Co. (Rahway, NJ)
- …commercial teams and cross divisional teams including R&D and manufacturing, medical affairs , Outcomes Research and AccessExecutional Excellence: Ability to ... years. Our company has launched a product in key US and Ex- US markets (Japan, China, EU)...hospitalization when added to the existing SOC.The Global Marketing Director , sGC Alliance, will lead key strategic elements to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …sales, medical /CMR, legal, compliance, and regulatory. Other internal relationships include Public Affairs , Government Affairs & US Corp Giving & Social ... independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships include… more
- Merck & Co. (North Wales, PA)
- …product planning team meetings with global marketing, US policy/ advocacy, US payer marketing, medical affairs , outcomes research , market ... Job DescriptionThe Associate Director will report directly to the US Marketing Leader for New Products and play a critical role in the US commercial… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory Affairs and other NNI skill ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...development, CMR is involved. The one thing that keeps us all marching to the same beat is our… more
- Tris Pharma (Monmouth Junction, NJ)
- …Inc. (www.trispharma.com) is a leading privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines ... addressing unmet patient needs. We have more than 150 US and International patents (including applications) and have marketed...opening in our Monmouth Junction, NJ facility for a Director , Drug Safety. The Director , Drug Safety… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Market Access and Public Affairs , and internal stakeholders from Marketing, Medical Affairs , HEOR, Finance, Commercial, Field Sales, Government Pricing, and ... role is based in Plainsboro, NJ. The Position The Director Market Access Channel Strategy is part of a...and long-term business objectives Ensures close collaboration with MAPA, Medical Affairs , HEOR, Marketing, Finance, and Field… more
