- Merck & Co. (North Wales, PA)
- …At least 3 years regional medical affairs experience (eg, Regional Director Medical Affairs) with proven track record of contribution to medical ... Job DescriptionGlobal Senior Director Medical Affairs (GDMA), Global Therapeutic Area Oncology-Gynecological MalignanciesThe Global Senior Director Medical … more
- Merck & Co. (Rahway, NJ)
- …technical platforms for the collection, review, and dissemination of medical informationScientific/medica and research experience, including demonstrated record ... Job DescriptionThe Regional Medical Scientific Senior Director - Team Lead (RMSD...protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with… more
- Merck & Co. (North Wales, PA)
- … medical affairs or clinical development experience with proven track record of contribution to medical or clinical development strategiesCustomer expertise, ... DescriptionThe Executive Director Pulmonary Hypertension, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) (referred to as EDMA) is… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with the ... Global Medical and Scientific Affairs Therapeutic Area (GMSA TA) teams...of strategic initiatives as evidenced by a successful track record of design/creation of and accountability for implementation of… more
- Merck & Co. (Sacramento, CA)
- …Practice (GCP) guidelines, and administrative/operational responsibilitiesPreferred Field-based medical experienceResearch ExperienceDemonstrated record of ... Job DescriptionThe Regional Medical Scientific Director (RMSD) is a credentialed (ie,...protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with… more
- Legend Biotech USA, Inc. (Houston, TX)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Senior Medical Science Liaison as part of the Medical Affairs team based in ... Houston, TX (remote). Role OverviewAs part of the US Medical Affairs team, the Senior Medical Science...highly preferred.A valid US driver's license and clean driving record are required.Ability to drive to or fly to… more
- Merck & Co. (Cincinnati, OH)
- Job DescriptionThe Virology (HIV) Regional Medical Scientific Director is a credentialed (ie, MD, PhD, DNP, or PharmD) therapeutic and disease area expert who ... when requested, with external scientific leaders and investigators in the medical and scientific community. - Virology RMSDs provide Scientific Leaders (SLs)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director, Medical Affairs QA, the Director of Medical Affairs QA is responsible for… more
- Daiichi Sankyo, Inc. (San Francisco, CA)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Summary: Daiichi Sankyo, Inc. (DSI) is currently seeking a Medical Science Liaison (MSL) to join the Field ...Must have a valid driver's license with a driving record that meets company requirementsAbility to travel up to… more
- Merck & Co. (Rahway, NJ)
- …Biological Sciences, Nursing, Pharmacy, Mathematics, Economy, Statistics, Computer Science, Medical Sciences is preferred.Knowledge - SkillsWork objectively and as a ... to deliver measurable impact in commercial pharma landscape.Knowledge in mining medical claims, consumer data with a strategic/inquisitive mindset and proven … more
- Merck & Co. (North Wales, PA)
- …experience in drug development or biomedical research experience in academiaDemonstrated record of scientific scholarship and achievementA proven track record ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (North Wales, PA)
- …experience in drug development or biomedical research experience in academiaDemonstrated record of scientific scholarship and achievementA proven track record ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (Boston, MA)
- …in academiaDemonstrated success in overseeing clinical studies and protocolsDemonstrated record of scientific scholarship and achievementProven track record ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (Boston, MA)
- …of decision making for drug development and as CDxDemonstrated track record in the development of CDxDemonstrated expertise in molecular diagnostic development ... as evident by peer review publication record , patents, and/or productsExperience influencing without direct authority, navigating complex or matrix organizations and… more
- Merck & Co. (TX)
- …and may also include surrounding towns, suburbs, and other nearby communities.1. Houston Medical Center, TX: Houston, TX; Pasadena, TX; Pearland, TX2. Houston N, TX: ... within healthcare or scientific fields such as pharmaceuticals, biotechnology, or medical devices.S2 Level: Bachelor's degree (BA/BS), or High school diploma or… more
- Merck & Co. (Buffalo, NY)
- …sector.Solid understanding of Rx Pathways, and prior authorization process.Track record of leading successful product launch teams in competitive markets.Proficient ... selling and leading teams in the Pharmaceutical, Biotech, or Medical Device industriesSkilled at establishing and maintaining relationships and networks… more
- Merck & Co. (Rahway, NJ)
- …related to container closure integrity and dose accuracy, among others.Proven track record of applying analytical skills in product test method design, development, ... guidance & standards: 21 CFR Part 421 CFR 82021 CFR 210/ 211EU Medical Device RegulationUSP USP FDA Guidance for Industry, Container Closure Systems for Packaging… more
- Merck & Co. (Rahway, NJ)
- …with at least 11 years of experience), where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (Rahway, NJ)
- …Practice (GMP) manufacturing support, familiarity with manufacturing batch record reviews and/or operations.Experience with mathematical modeling, theoretical ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
- Merck & Co. (Rahway, NJ)
- …digital pathology algorithms.Excellent oral and written skills with a proven record of scientific contributions to the scientific community.Demonstrated ability to ... protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.-… more
