- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …as other research areas centered around rare diseases and immune disorders. Summary The Director, Clinical Safety, will be a product safety lead or part of a ... product safety team, and be responsible for overall product safety strategy or specific areas of...may function as a key member of the Global Product Team in collaboration with Clinical Development,… 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 ... education and collecting data to support efficacy and new product development, CMR is involved. The one thing that...This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that… more
- Aequor (NJ)
- …local candidates as well) Required bachelor's degree Must Haves: Phase 1 to 4 clinical trial experience Managing end to end supply chain Job Description: 100% ... Study Teams as well as cross-functional teams. Proactively defining, planning, and communicating clinical supply strategy in support of global clinical … more
- Novo Nordisk Inc. (Cincinnati, OH)
- …Team leads the US sales efforts for Novo Nordisk's robust cardiometabolic product portfolio, which includes world class therapies for the treatment of diabetes, ... insights that drive our business forward. You will drive the NNI portfolio strategy in tandem with our marketing team, and balance performance with compassion to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …GTL is the GPT Leader, directly accountable for conceiving, designing and implementing product development strategy and delivery for their asset(s). The GTL has ... will have to lead a complex, global team in charge of a global clinical program designed to support registration and develop value-enhancing life-cycle strategy .… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to ensure that the most up-to-date information on the therapeutic area and NNI clinical plans and study results, product support letters, and the Marketing and ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...education and collecting data to support efficacy and new product development, CMR is involved. The one thing that… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders.Summary Lead the implementation of the quality strategy closely aligned with the business strategy within one or more ... Business Units. Provide strategic and proactive QA Leadership for respective GPTs and Clinical Programs in close alignment with the Head of R&D QA. Within assigned… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …excess of $900M annually Works effectively with international colleagues for new product launches Cross functional collaboration: Ensures strategy alignment of ... the US marketing efforts for Novo Nordisk's robust cardiometabolic product portfolio, which includes world class therapies for the...media experts to develop, implement and optimize paid media strategy across Patient, HCP, Trade, EHR and other NNI… more
- Merck & Co. (Rockville, MD)
- …or elsewhere, and identifying those issues likely to impact the company's regulatory strategy or product portfolio.Leading internal teams as assigned to address ... Research Laboratories divisions and most directly with Global Regulatory Affairs and Clinical Safety (GRACS) to define and implement a prioritized plan for policy… more
- Merck & Co. (Rahway, NJ)
- …activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …strategies for the assigned asset. This person will own the pricing and access strategy for the assigned oncology asset(s). This person will report to the Sr ... indications. With manager oversight, the individual will lead global pricing strategy development, access strategy development and partner with stakeholders… more
- Merck & Co. (North Wales, PA)
- …activities for multiple and/or large/complex late stage drug/vaccine clinical development projects.- Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… 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 ... requirementsTypically has administrative responsibility for recruiting, retaining, developing, and managing employeesGuide career growth and provide development opportunity for… more
- Merck & Co. (Rahway, NJ)
- …interaction with all areas of the business including communications, clinical development, manufacturing and supply, regulatory, business development, marketing, and ... commercial groups.Responsibilities include but are not limited to: Managing a large worldwide trademark portfolio, including counseling, clearance, filing, and… more
- Merck & Co. (North Wales, PA)
- …be based in either Rahway, NJ; Upper Gwynedd, PA. Primary Responsibilities: Managing the end-to-end drug development process including projects that are of moderate ... includes integrating strategic and tactical input from diverse disciplines (eg, clinical , regulatory, market access, manufacturing, CMC, commercial, and other areas)… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …partnerships with business leaders and demonstrates operational excellence in managing multiple complex and competing priorities simultaneously. Proven project ... management and strategy skills. Is experienced in leading complex initiatives of...keep informed of industry trends and newsworthy happenings, company product pipeline progress, and overall financial position of the… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …responsible for developing and executing an asset's CMC (Chemistry Manufacturing & Controls) strategy . This is a growing organization that was formed within the past ... aggregating individual program information to a portfolio viewEstablish robust CMC and clinical stakeholder interfaces to maintain a pulse on all programs within the… 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 ... requirements.Typically has administrative responsibility for recruiting, retaining, developing, and managing employees. Guide career growth and provide development opportunity… more
- EY (Dallas, TX)
- …experience and physician experience (for example working on the transformation of clinical services and product solutions, including technology and workflow ... Health and SC practice, helping clients with strategic growth, business, clinical and technology transformations. This senior role within our Consulting practice… more
