- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire...to manage future or ongoing clinical research projects. Qualifications Education MD, DO, MD/Ph.D, or DO/PhD.. Required Must have… more
- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, New Jersey, Tris has an immediate opening for a full-time permanent Director / Senior Director , Clinical Quality Assurance. This is a hybrid ... Title commensurate with experience.SUMMARY:Reporting to the Chief Quality Officer the Senior Director of Clinical Quality Assurance provides strategic leadership… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders.SummaryThe Senior Director , Global Oncology Medical Affairs, Evidence Generation role ... able to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- PharmD, PhD or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an ... meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- MD required-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an ... to meet the qualifications below with or without a reasonable accommodation. Education : (from an accredited college or university)MD requiredPostgraduate training in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, ... meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)- Bachelor's Degree Life… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …defining key scientific questions and plan. Align closely with the Senior Translational Strategy Lead.Construct translational plan documents, biomarker data analysis ... able to meet the qualifications below with or without a reasonable accommodation. Education :PhD, PharmD or MD degree required Experience:10 or more years of… more
- Merck & Co. (Rahway, NJ)
- …innovative statistical methods and applications in clinical trial development. Education and Minimum Requirement: PhD or equivalent degree in ... work location and the chosen candidate's relevant skills, experience, and education . Expected US salary range: $181,600.00 - $285,800.00Available benefits include… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)Bachelor's Degree ... requiredAdvanced degree (eg, Masters, Pharm.D., Ph.D.) in a scientific discipline preferred Experience Qualifications10 or More Years Experience in the pharmaceutical industry7 or More Years with direct regulatory affairs experience, including experience in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …limited to protocol amendments, Dear HCP letters and key medical education initiatives.Develops prospective contingency plans for management of assigned safety risks ... setting.Contributes to creation and improvement of Clinical Development processes. Education :MD required; prefer Board certification in Oncology. Experience:At least… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Serves as RA CMC representative supporting company initiatives. Qualifications: Education and Experience:Bachelor's Degree in Life Science required.M.S./PhD. ... preferred in a scientific discipline. MS Degree with 8-10 years pharmaceutical industry experience with 4+ years direct or related CMC regulatory experience orPhD. with 6-8 years pharmaceutical industry experience and 4+ years direct or related CMC regulatory… more
- Merck & Co. (Washington, DC)
- Job DescriptionPosition Description: Director , Global Policy and Multilateral Engagement The Director , Global Public Policy and Multilateral Engagement is ... key industrial policy issues under consideration by multilateral organizations (MLO).The Director leverages their networks to further goals aligned with our… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Key Opinion Leaders (KOLs), Healthcare Professionals (HCPs), and other stakeholders. The Medical Director will also assist the Senior Medical Director in ... implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...Area in certain instances, at the discretion of Executive Director of Medical Affairs. Assists the Senior … more
- Merck & Co. (North Wales, PA)
- …affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior Director , Executive Director , and/or Associate Vice ... and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the planning and… more
- Merck & Co. (Rahway, NJ)
- …manufacturing to manage clinical development projects; and assist the Senior /Executive Clinical Director /Vice-President in ensuring that appropriate corporate ... Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning...to manage future or ongoing clinical research projects.Qualifications / Education :M.D., DO, MD/Ph.D, or DO/PhD.Required:Minimum of 5 years of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for effectively ... wide range of functions in Daiichi Sankyo (DS). Reporting to the Sr. Director , Enterprise Program Management, this position requires a capable leader with strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the Senior Director , GMA Oncology ADC (Global Medical Affairs team lead for ... education and other scientific exchange activities in alignment with the Senior Director , such as scientific symposium and medical congresses, within legal… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director , Lab Management Our team in Rahway, New Jersey, is seeking a strong leader who is passionate about lab ... management and operation support. The Associate Director of Biologics Process Research and Development (BPR&D) is...and Company EHS, serving as a liaison and representing senior administration on EHS/chemical hygiene committees. The candidate is… more
- Merck & Co. (North Wales, PA)
- …Director , GLOBAL REGULATORY CMC Biologics (R5)Under general supervision of an Executive Director / Senior Director , the Principal Scientist / Director is ... support of their assigned projects. Position Description- The Principal Scientist / Director responsibilities include but are not limited to:Serve as a Regulatory… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
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