- DivIHN Integration Inc (Columbus, OH)
- …regional contract CRAs, and organizes the files and budgets associated with several clinical studies . Provides medical support which may include: Adverse Event ... investigation of medical adverse events and works with Medical Affairs , Clinical , and Regulatory Affairs ...safety issues concerning foods or products and, by supporting clinical study teams with safety-related aspects and… more
- Merck & Co. (Rahway, NJ)
- …Director, Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic community to ... congressesLeads our Company's global scientific input forums to gain external scientific / clinical insights in support of our Company's R&D strategySustains… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …toGMA clinical operations teams as part of evidence generation forums and study teams for Local/Regional Medical Affairs company sponsored study concepts ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...and immune disorders.Summary The Senior Director, Global Oncology Medical Affairs is responsible for developing the Global Medical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … clinical activities as appropriate.Responsibilities Clinical Operations Study / Program ManagementCompany Sponsored Studies (CSS) Support the preparation, ... quality in the execution of all Global Oncology Medical Affairs (GOMA) Company Sponsored Studies (CSS) and...and execution and reporting of all global oncology medical affairs operations clinical trial activities, ensuring adherence… more
- Merck & Co. (North Wales, PA)
- …headquarters-based position in Our Company Research Laboratories Global Medical and Scientific Affairs (Research & Development (R&D) GMSA). Responsibilities and ... & Biomarkers will be responsible for driving execution of scientific & medical affairs plans for their...to medical affairs strategiesExperience in country/region medical affairs or clinical development (in IBD or… more
- Eisai, Inc (NJ)
- …within ESI. Continuously update plans and inform stakeholders of progress.Phase IV Clinical Studies : Direct and design strategies, planning and implementation of ... Responsible for approval of medical and scientific content of Regulatory, Safety, Scientific Affairs , Medical Affairs and Commercial outputs for assigned… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …insights.- Serve as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document ... level is required.- Knowledge in and understanding of Global Medical Affairs activities (including scientific communications, medical information, evidence… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Position The Therapy Area (TA) head is accountable for setting an integrated medical affairs strategy, scientific engagement plan and execution of that plan for ... customer needs. Relationships The position reports into VP, Medical Affairs and will have all relevant in-house and field...most up-to-date information on the therapeutic area and NNI clinical plans and study results, product support… more
- Merck & Co. (Los Angeles, CA)
- … Directors specific therapeutic area.ResearchUpon request from Global Center for Scientific Affairs (GCSA),Initiates discussions with SLs and/or potential ... diversityConsistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating… more
- Daiichi Sankyo, Inc. (Nashville, TN)
- …Experience:MSL/Sr. MSLExperience Qualifications:1 or More Years' experience including medical & scientific affairs , clinical practice, research, academic or ... Director MSLExperience Qualifications:5 or More Years' experience including medical & scientific affairs , clinical practice, research, academic or… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …internal stakeholders using trackers and tools generated by Global Oncology Medical Affairs Study Operations partners and propose mitigation plans for delayed ... Country Medical Affairs required- Experience planning and conducting Medical Affairs interventional and non-interventional studies , including Ph 3b/4, EAP,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …internal stakeholders using trackers and tools generated by Global Oncology Medical Affairs Study Operations partners and propose mitigation plans for delayed ... Country Medical Affairs required- Experience planning and conducting Medical Affairs interventional and non-interventional studies , including Ph 3b/4, EAP,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …testingAt the time of implementation of a CDx study /IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once ... by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and… more
- Merck & Co. (Rahway, NJ)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint ... may:Supervise the activities of Clinical Scientists in the execution of clinical studies ;Work closely with a cross-functional group of experts in… more
- Taiho Oncology (TX)
- …training meetings, and communication of scientific insights for specific studies from clinical sites to internal TOI departments. Professional Organization ... care practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The MSL integrates clinical / scientific expertise and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …including NNI Evidence Generation Plans and Product Development Plans Clinical study management: Provide regional medical & scientific input on trial ... clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4)...Internal relationships include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory … more
- Eisai, Inc (Nutley, NJ)
- …ESI. Continuously update plans and inform stakeholders of progress. 30%Phase IV clinical studies : Direct and design strategies, planning and implementation of ... Responsible for approval of medical and scientific content of Regulatory, Safety, Scientific Affairs , Medical Affairs and Commercial outputs for assigned… more
- Merck & Co. (South San Francisco, CA)
- …experience.Required Experience and Skills: Strong writing skills and experience drafting study reports, scientific manuscripts, or scientific documentsStrong ... writing and preparing nonclinical pharmacology regulatory document submission sections and study reports to support the development of therapeutic agents and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …indications.Support as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the Senior… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Affairs , Medical Strategy & Operations, Medical Information, Publications, Clinical Directors, HEOR Directors, Global Medical Directors, Marketing, and Market ... Review and provide comments to trial outlines/protocols for Novo Nordisk-sponsored clinical trials Review proposals for investigator-sponsored studies (ISS) and… more
