- Novo Nordisk Inc. (Plainsboro, NJ)
- …directly into the TA head). They will coordinate with other TA functions including Medical Directors, Alignment Director , Program Development Director ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...analytic support to the field team, and assists the Program Development and Training function for the TA. SD… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … Affairs team lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs ... research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …directly into the TA head). They will coordinate with other TA functions including Medical Directors, Alignment Director , Program Development Director ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...analytic support to the field team, and assists the Program Development and Training function for the TA. SD… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized ... of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.Looking for someone with… more
- Merck & Co. (North Wales, PA)
- … monitoring team in review and interpretation of clinical data/ medical protocol-deviations in collaboration with the Clinical Director .Builds talent and ... and execution of Phase 1-4 clinical studies.-Under the direction of the Program Lead, you will collaborate with global, cross- functional team-members including… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …clinical trial performance and quality metrics and share with study team, Operations Program Lead, and Sr. Director for the compound, on regular basis ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...against trial progress and bring deviations to the Operational program Lead and study team leader. Review … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … Affairs team lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select Medical Affairs ... research areas centered around rare diseases and immune disorders. Job Summary:The Director , Global Medical Affairs (GMA), Gyn Oncology, under the direction… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you.The Sr Medical Director provides medical leadership for medical affairs strategy, ... medical advisory boards, and scientific communication/publication components of overall medical operating plan.The Sr Medical Director provides strategic… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Represents Clinical Development in Project Teams, possibly as Global Clinical Lead.Responsibilities: Medical Monitoring Planning (MD Only): For large Phase 2 or Phase… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …coding of AEs, medical history, and medications when needed- Addresses medical questions directly from sites/ Institutional Review Boards (IRBs), and other ... Monitor (MM):- Provides oversight to the CRO MM for clinical data review activities- May support addressing eligibility and medical questions from sites/… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …DS stakeholders on the disease area and compound/DrugMay serve as speaker for program / franchise medical /scientific training - Guide the Clinical Science staff ... multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective programThis Clinical Science (CS)...(CS) Group Lead will be responsible for overseeing multiple program -level CS Asset Leads who are managing a team… more
- Insmed Incorporated (Bridgewater, NJ)
- …with Regulatory project leads in the US, EU, and Japan, the Director , Regulatory Labeling will be responsible for creating (and/or updating) labeling content, ... guiding internal review , and facilitating the approval process for labeling content...pet, legal, and supplemental life insuranceFlexible spending accounts for medical and dependent careAccident and Hospital Indemnity insuranceEmployee Assistance… more
- Insmed Incorporated (Bridgewater, NJ)
- …Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewAssociate Director , Tech Ops (Process Chemistry) will have responsibility for the ... process.Responsible for technical support as Insmed's internal SME, technical review of quality documentation, management of schedule/raw material consumption/budgets,… more
- Catalent (Harman, WV)
- Senior Director , Supply Chain Position Summary: The Senior Director , Supply Chain is responsible for leading the supply chain organization for Catalent Maryland. ... to the Vice President and General Manager, the Senior Director Supply Chain directs all facets of supply chain...you should join Catalent:Defined career path and annual performance review and feedback process.Potential for career growth on an… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... learner-obsessed with experience in developing and managing a learning program from content to delivery. ** Prior to applying,... from content to delivery. ** Prior to applying, review the Education & Qualification section - Be sure… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …operational topics among leadership and stakeholders.Support, where needed, internal program /study review meetings preceding governance investment decision ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and immune disorders.SummaryOversees a number of trials of a multinational program in a specific indication, ie, multiple multinational phase II/III clinical… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... CDx project teams for the diagnostic, in full alignment with Global Program Teams (GPT) for the therapeutic, covering all areas from CDx assay… more
- Insmed Incorporated (Bridgewater, NJ)
- …Agreements in compliance with Clinical Development Plans and regulatory requirements.Provide program level medical oversight of information included in ... the NDA/CTD submissions, and responses to questions from regulatory authority or EC/IRBs.Provide medical feedback for activities related to review of data for… more
- Insmed Incorporated (Bridgewater, NJ)
- …New York™, and Best Workplaces for Millennials™ lists.OverviewReporting to the Executive Director Quality GMP Compliance, the Director , Quality Operations will ... of compliance requirements, work with critical suppliers to ensure quality, consistent supply. Review and monitor all lab processes to ensure they follow relevant… more
