- Daiichi Sankyo, Inc. (Bernards, NJ)
- …industry with expertise in the involvement of regulated activities for medical affairs , or clinical development. requiredMust possess a solid understanding of ... authority regulatory requirements particularly in the areas of Medical Affairs and Clinical Development; Must have a strong understanding of pharmaceutical drug… more
- Merck & Co. (Salt Lake City, UT)
- …Work Arrangements:RemoteShift:Not IndicatedValid Driving License:YesHazardous Material(s):n/aRequired Skills:Accountability, Clinical Affairs , Clinical ... Studies, Clinical Trials, Data Analysis, Leadership, Medical Affairs , Medical Relations, Pharmaceutical Medical Affairs -Preferred Skills:Job Posting End… more
- Eisai, Inc (Nutley, NJ)
- …plan. Provide strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department for ... in relevant therapeutic area.Substantial experience across areas of Medical Affairs ' functions or phase II/III/IV clinical trials...of Medical Affairs ' functions or phase II/III/IV clinical trials and diseases in the therapeutic area is… more
- Merck & Co. (Cincinnati, OH)
- …reports to the Regional RMSD Team Leader - within US Medical Affairs , Global Clinical Development, Research and Development (R&D).--Primary Activities:Identify, ... Clinical Testing, HIV AIDS, Investigator-Initiated Studies (IIS), Medical Affairs , Pharmaceutical Medical Affairs , Professional Integrity, Professional… more
- Daiichi Sankyo, Inc. (San Francisco, CA)
- …MSL/Sr. MSL1 or More Years' experience, including medical & scientific affairs , clinical practice, research, academic or US-managed markets preferredPrevious ... MSL/Associate Director MSL5 or More Years' experience including medical & scientific affairs , clinical practice, research, academic or US managed markets… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of the Global Scientific and Medical Affairs Plans ... Cycle Management decisions. In addition, the leads the Medical Affairs input into the Value and Evidence Plan (V&I)...asset value proposition, insights from affiliates and regions, and clinical and value evidence gaps. Translate these Goals and… more
- Merck & Co. (Rahway, NJ)
- …and reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial, and ... and promotion of our company's products.Develops a strong matrix relationship with clinical development, medical affairs , market access, commercial, and key… more
- Merck & Co. (Rahway, NJ)
- …with Global Clinical Trial Operations (GCTO) and the broader Global Clinical Development (GCD)-Coordinates with Global Medical Scientific Affairs to ensure ... Job DescriptionThe Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with the… more
- Eisai, Inc (Nutley, NJ)
- …of clinical studies in relevant therapeutic area.Experience across areas of Medical Affairs ' functions or phase II/III/IV clinical trials and diseases in the ... from you. The Associate Medical Director, US Oncology Medical Affairs - Women's Cancer assists in the development of...planning, implementation, and oversight of Phase I through IV clinical trial programs and early new product development within… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Executive Director, Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic ... studies program in partnership with late-stage development teams in Medical Affairs while also supporting early-stage development teams. The role also partners… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Director, Regulatory Affairs will serve as the regulatory leader on cross-functional teams, ... to cross-functional teams and senior leadership, as neededCollaborate with Clinical Development, Clinical Operations, CMC, QA/QC, Nonclinical, Program… more
- Eisai, Inc (Nutley, NJ)
- … studies in relevant therapeutic area. Substantial experience across areas of Medical Affairs ' functions or phase II/III/IV clinical trials and diseases in the ... from you. The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics for assigned therapeutic area. This role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. SummaryThe Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology ... (US Medical Affairs team lead for compound), is responsible for assisting...compound.- Responsible for scientific communications and publications; interpretation of clinical data; ensuring consistency of clinical content… more
- Insmed Incorporated (San Diego, CA)
- …closely with the Biometrics teams, Clinical Operations teams, Clinical Development teams, Regulatory Affairs , and external partners.ResponsibilitiesEDC ... will lead and oversee EDC programming, and database build for in-house clinical trials. This role will be responsible for the development and implementation… more
- Insmed Incorporated (St. Louis, MO)
- …insights to Insmed. Support research and development programs as requested by R&D, Clinical Operations, and Medical Affairs Departments. This may include trial ... to internal Insmed colleaguesFull support and execution of Medical Affairs plans, Clinical Development projects, programs, and initiativesQualifications:An… more
- Merck & Co. (Upper Gwynedd, PA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; ... --The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director has… more
- Merck & Co. (Rahway, NJ)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory… more
- Merck & Co. (Rahway, NJ)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's… more
- Merck & Co. (Rahway, NJ)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Merck & Co. (Boston, MA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
