- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study Team Leader for ... disorders. Job Summary: The incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global ... make decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Director , Clinical Informatics in the Clinical Data Science & Evidence (CDSE) ... department develops clinical and medical informatics software and system development with customers in collaboration with the research partnerships function of… more
- Genmab (Plainsboro, NJ)
- …Operations & System team and our cross-functional stakeholders.Together with Global Clinical Drug Supply Operations & Systems team the three teams make ... authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of Global … more
- Genmab (NJ)
- …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight to ... and the drug development processSignificant experience leading data management activities in clinical trials; advanced use of data management systems ; advanced… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the CMR organization. This individual will serve as a subject matter expect on clinical and medical informatics software and system development with customers in ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...medical informatics preferred Solid understanding of the US Healthcare system Strong interpersonal, collaborative, relationship building and communication skills… more
- Genmab (Plainsboro, NJ)
- …with the Global Clinical Drug Supply Planning team. Together with the Global Clinical Drug Supply Systems team, these groups form the Global Clinical ... and a can-do attitude to achieve results.You will be reporting to Director , Global Clinical Drug Supply in Copenhagen, Denmark.Main Responsibilities… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory Affairs & ... Clinical Safety global business processes. This includes defining and...process for their respective global business processes (eg, enabling systems , upstream and downstream transfer of information and assets).Accountable… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - RWE ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...ready to make a difference? The Position The Associate Director , Research Partnerships (RP) is responsible for developing and… more
- Genmab (NJ)
- …RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early and ... responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Merck & Co. (North Wales, PA)
- …effectively work across a heavily matrixed organizationKnowledge of US healthcare system , national and society treatment guidelines, clinical research processes, ... Job DescriptionRole Summary The Hematology US Scientific Director , Medical Affairs (SDMA) is a regionally based... of Medical Affairs (RDMA) (where applicable), US Global Clinical Trial Organization, Global Medical and Scientific Affairs (GMSA)… more
- Merck & Co. (Lower Gwynedd, PA)
- …financial and operational objectives for the Regulated Robotics teamDrives the computer system validation efforts for all departmental automation systems and ... scientific and technical expertise in regulated assay design, automation, development, LIMS systems , system validation, and execution of these in support of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... manage cross-functional study team, external service providers (CROs, vendors, etc.) and clinical sites to ensure all trial deliverables are met according to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing scientifically ... accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This...strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... for a living. Are you ready to make a difference? The Position The Senior Director of CMR Knowledge & Technical Advancement (KTA) Department will serve to act as an… more
- Merck & Co. (Lower Gwynedd, PA)
- …of a variety of automated processing and operational and informational technology systems .Apply deep expertise in the computer system validation process of ... staff while building and maintaining strong working relationships.Serve as a system administrator of equipment applications, temperature monitoring systems , and… more
- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will report to the Senior ... Director , US Medical Affairs Solid Tumors Strategy Lead. S/he...market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross functional teams.We have… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Development SOP Management Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... centered around rare diseases and immune disorders. Job Summary: The Director , Development SOP Management is responsible for providing strategic direction, planning,… more
- Merck & Co. (Rahway, NJ)
- …Reporting to the AVP Global Market Access, Global Pharma, the Executive Director , Global Market Access, Infectious Disease & Ophthalmology will be a member ... team and will lead a team across the ID&O portfolio.T he Executive Director , Global Market Access, Infectious Disease & Ophthalmology will play a leadership role… more
- Merck & Co. (Rahway, NJ)
- …the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical ... Job Description Director -QP2-IO We are seeking an experienced talented...clinical trial design simulation, disease progression models, quantitative systems pharmacology (QSP) modeling, and comparator modeling. Strategizing and… more
Related Job Searches:
Clinical,
Clinical Director,
Clinical System,
Director,
Director Clinical System Development,
Director Clinical System Services,
Director System,
Director System Clinical Pharmacy,
System