- Eisai, Inc (NJ)
- …this is your profile, we want to hear from you. Job Summary The Associate Director , Clinical Outsourcing, will oversee and lead and support activities related to ... Salary Transparency Language:The base salary range for the Associate Director , Clinical Outsourcing is from :157,200-206,300Under current...and as such, is committed in policy and in practice to recruit, hire, train, and promote in all… more
- Eisai, Inc (Nutley, NJ)
- …required.#LI-MI1#IND123#LI-RemoteEisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Data Science - CEG is from ... your profile, we want to hear from you. The Clinical Data Science team at Eisai, Inc., is expanding...and as such, is committed in policy and in practice to recruit, hire, train, and promote in all… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in the assigned therapeutic area. Relationships Reports to the Executive Director - Clinical Research & Development. Internal relationships include working ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...activities: Stay abreast of guidelines, current trends and medical practice in the assigned therapeutic area, including reports and… more
- Novo Nordisk Inc. (Chicago, IL)
- …Clinician in appropriate specialty (CVR) preferred At least 5 years in clinical practice and/or relevant industry expereince required Extensive Disease state ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...ready to make a difference? The Position The Scientific Director (SD) functions as a subject matter expert to… more
- Insmed Incorporated (Bridgewater, NJ)
- …the biopharma industry, come to Insmed to accelerate your career. OverviewThe Director of Field Medical Excellence (FME) will develop field medical functional ... high-quality, impactful customer engagements with a consistent approach worldwide. The FME Director will also drive operational excellence across the regions. The … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …in pharma at local, regional and/or Global level. preferredExcellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other ... areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the Senior… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …the commercialization of oncology products is required.- Excellent knowledge of current clinical practice and treatment landscape in Oncology, specifically for ... research areas centered around rare diseases and immune disorders. Job Summary:The Director , Global Medical Affairs (GMA), Gyn Oncology, under the direction of the… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical affairs strategy, planning and ... communication/publication components of overall medical operating plan. The Medical Director provides strategic development, planning, implementation and oversight of… more
- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... tactics for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for ... implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's publication policies… more
- Eisai, Inc (Nutley, NJ)
- …this is your profile, we want to hear from you.The Sr Medical Director provides medical leadership for medical affairs strategy, planning and supportive tactics ... communication/publication components of overall medical operating plan.The Sr Medical Director provides strategic development, planning, implementation, and oversight of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …negotiations in accordance with all relevant regulations and policies; (Good Clinical Practice (GCP), ICH guidelines, federal regulations (Sunshine/Open Payments ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...ready to make a difference? The Position The Assoc Director OED - Supplies, is responsible for US and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …through peer-to-peer interactions, as needed Stay abreast of evolving regulatory requirements, clinical guidelines and current trends in medical practice Remain ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...evidence-based M&A advisory services. Reporting into the Senior Medical Director , M&A Scientific Advisory, the Medical Director ,… more
- Merck & Co. (Rahway, NJ)
- …of, contractors performing various GMP activities supporting the production of clinical supplies with focus on drug product. Additionally, experience in medical ... expertise.- Leads others in a matrix/management environment.Lead the resolution of business practice , Quality and/ or compliance issues of broad scope and highest… more
- Eisai, Inc (Nutley, NJ)
- …understanding of statistical methodologies and their application in the context of non- clinical studies and related projects in AD and other therapeutic areas as ... deliverables and timelines within GV&A projects related to both clinical trial setting and observational studies.Serve as the lead...and as such, is committed in policy and in practice to recruit, hire, train, and promote in all… more
- Catalent (Philadelphia, PA)
- Position: Director QualityLocation: Philadelphia, PAPosition Summary: The Quality function is to build, monitor, and sustain a robust and effective quality system ... and guidance world-wide, including but not limited to, good manufacturing practice /quality system requirements of the Food and Drug Administration, state boards… more
- Eisai, Inc (Nutley, NJ)
- …describe complex disease processes to understand and evaluate the implications of clinical trials and real-world data; demonstrate the value of interventions beyond ... is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of analysis data sets and tables, listings, and figures (TLFs) needed for clinical study reports and regulatory submissions, as well as in-house validation of this ... initiates writing of global standard operating procedures for statistical programming practice , especially with respect to oversight of vendor performance. Oversees… more
- Merck & Co. (North Wales, PA)
- …affairs organization's strategy within the therapeutic area. The MCRP also leverages clinical practice and therapeutic area expertise to participate in the ... global assurance process for country assessment.US and Global Medical Information-Leverage clinical practice & therapeutic area/product expertise to provide… more
- Lundbeck (Chicago, IL)
- …engaging US KOLs in relevant therapeutic areas, consolidating and communicating key US clinical practice and healthcare system insights Liaise with US New ... US medical insights for assessment of global Lundbeck BD opportunities and pipeline clinical development. Furthermore, the Sr Med Dir will build the US MA's future… more
