- Merck & Co. (North Wales, PA)
- … Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. ... business about twenty (20) percent of the time to manage future or ongoing clinical research projects. Education MD or MD/Ph.D. Required Qualifications Must have… more
- Merck & Co. (Boston, MA)
- …execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and ... Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed...medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (MA)
- …execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and ... Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology.… more
- Merck & Co. (Upper Gwynedd, PA)
- …--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 primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... to bring new treatments to patients faster and more efficiently.About the PositionThe Senior Director, Regulatory Affairs lead is responsible for developing and… more
- Merck & Co. (South San Francisco, CA)
- …Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research ... clinical study support staff and scientists (including discovery research , biostatistics, drug metabolism, modeling and simulation, regulatory affairs,… more
- Genmab (NJ)
- …using R to support clinical trial preferred Demonstrated knowledge of clinical research , metadata management, industry standards (CDISC), FDA & ICH, GCP, ... like a fit? Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and… more
- Eisai, Inc (Nutley, NJ)
- …on clinical quality topics.Build and manage overall relationships with regulatory bodies to address emerging needs and issues.Manage and retain talent within ... 15 or more years significant clinical pharmaceutical experience (ie, clinical development or operations, regulatory compliance).Substantial experience in … more
- Insmed Incorporated (NJ)
- …lead over an 1-2 indications within one compound, in collaboration with the Senior Director, Clinical Operations. Ensures consistent and successful execution of ... and minimum of 7 yrs managing direct reports. Experience considered relevant includes clinical or basic research in a Pharmaceutical company, Academic … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …medical affairs, and regulatory affairs Maintain training assignments on clinical research documentation, regulatory requirements, Good Clinical ... global regulatory requirements Coordinate mandatory compliance training for clinical research staff, including GCP certification and recertification programs… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …a key member of the Global Product Team in collaboration with Clinical Development, Regulatory , Project Management, Biostatistics, Pharmacology, and other ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Under the Group's… more
- Merck & Co. (Rahway, NJ)
- …- #eligibleforERP GCSCareer25 #PSCSRequired Skills: Adaptability, Change Management, Clinical Research , Cross-Functional Team Leadership, Data Analysis, ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company Research Laboratories portfolio of… more
- Merck & Co. (Upper Gwynedd, PA)
- …organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research .Under the guidance of a senior leader, this position supports ... and barriers to reimbursement and market access, and provides input into clinical , regulatory , payer/access, marketing and evidence generation strategies and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …economics, epidemiology, outcomes research , public health, health services research , biostatistics, medicine, clinical research , biomedical sciences) ... About the Department The Clinical , Medical and Regulatory (CMR) department...a minimum of 4 years of experience in similar clinical /medical/ research departments in Pharmaceutical Industry, in health… more
- Merck & Co. (North Wales, PA)
- …of an Executive Director, within the Value and Implementation, Outcomes Research the incumbent has the following responsibilities:1) development of the integrated ... and/or vaccines on a worldwide basis and3) development and implementation of Outcomes Research (OR) and Real World evidence programs to meet the value evidence needs… more
- Formation Bio (New York, NY)
- …pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines ... with strong IP potential, and thereafter coordinate patent and regulatory activities to deliver best-in-class IP positions. We expect...Why Join Us? Impact: Shape IP strategy as our senior legal leader for a portfolio of clinical… more
- Merck & Co. (Rahway, NJ)
- … Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Company's Research and Development ... for clinical supplies. Interacts with key partner organizations such as clinical development, regulatory , quality and other supply chain areas to address… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …years work experience with Bachelors degree required- Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryAssist in planning… more
- Merck & Co. (North Wales, PA)
- …responsible for the formulation and execution of automation strategy in Global Clinical Trial Operations and all the support activities within their functional area. ... This includes working with stakeholders across Global Clinical Trial Operations (GCTO)and other relevant teams, driving the strategy from ideation to value… more
- Merck & Co. (North Wales, PA)
- …and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development ... keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.Responsible for continuous… more
