- Merck & Co. (Rahway, NJ)
- …GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The Associate Director will serve as a team member of the MACS Detailed Design ... high degree of technical and project management responsibility. The Associate Director - Process/Facility Lead position will... - Process/Facility Lead position will report to the Director , Engineering and will be a member … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs (GMA) Oncology- Medical Content ... is responsible for execution of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans… more
- Merck & Co. (Millsboro, DE)
- …for the humane care of animals at the Millsboro facilities. As the Associate Director , this individual is an active member of the Site Leadership Team and is ... to add an Attending Veterinarian in the role of Associate Director .This position will have overall responsibility...care staff, serving as a designated reviewer and voting member of the Institutional Animal Care and Use Committee… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... incumbent will champion model-based drug development as an active team member of clinical and development teams.ResponsibilitiesResponsible for all aspects of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights ... or PhD or other advanced degree is strongly preferred Experience Qualifications- 7 or More Years in Market Research,...worked in multiple regions and/or worked as Global Team member preferred Travel Ability to travel up to 20%… more
- Daiichi Sankyo, Inc. (Boston, MA)
- …other research areas centered around rare diseases and immune disorders. Summary: The Associate Director Field Reimbursement (ADFR) is a critical front-line ... or universityBachelor's Degree requiredMaster's Degree or other advanced degree preferred Experience Qualifications:7 or More Years overall related experience ,… more
- Daiichi Sankyo, Inc. (Seattle, WA)
- …other research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Field Reimbursement (ADFR) is a critical front-line ... or university) Bachelor's Degree requiredMaster's Degree or other advanced degree preferred Experience Qualification 7 or More Years overall related experience ,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a ... member of the Global Project Team (GPT) utilizing precedent and experience to develop innovative and flexible approaches to achieve development goals, advise on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the CMC sub team and the RA team and serves as ad hoc member to the Global Project Team for late stage projects. This position manages multiple biological ... as RA CMC representative supporting company initiatives. Qualifications:Education and Experience :Bachelor's Degree in Life Science required.M.S./PhD. preferred in a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with Global Regulatory Leads (GRLs). This position may serve as an ad hoc member of Global Project Team (GPT) to address labeling issues for late stage projects. ... discipline requiredadvanced degree (eg, Masters, Pharm.D. or Ph.D.) preferred Experience Qualifications7 or More Years pharmaceutical industry experience … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of ... or More Years with PharmD, PhD and relevant clinical experience preferred7 or More Years with Master's degree and...or More Years with Master's degree and relevant clinical experience preferred TravelAbility to travel up to 30%. In-house… more
- Insmed Incorporated (San Diego, CA)
- …Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , Quality Assurance - Analytical,GMP has responsibility ... requiredA minimum of 10 years of relevant Quality Assurance experience or similar function required Direct experience ...yearCompensation & BenefitsWe're committed to investing in every team member 's total well-being, now and in the future. We… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... of developing innovative cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo CAR-T cell therapy program.… more
- Insmed Incorporated (Phoenix, AZ)
- …Patient Support Program and the reason we are seeking top talent for the role of Associate Director of Case Management. Patients are the core of what we do here ... medications. Enhancing critical capabilities around the patient and HCP experience "post prescription" is the exact vision of the...so, we want to hear from you! As an Associate Director of Case Management, you will… more
- Insmed Incorporated (San Diego, CA)
- …Millennials™, and Best Medium Workplaces™ lists.OverviewJoin the Technical Operations team as Associate Director of MSAT where you will support pipeline programs ... or Pharmaceutical Engineering, or related field alongside significant leadership experience across Bioprocessing leadership and 8-10 years of work experienceBroad… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …team based in Raritan, New Jersey. Role OverviewThis position is a key member of the technical leadership function in the global MSAT organization. This individual ... related fieldMinimum 10 years of industrial biologics CMC development or manufacturing experience , CAR-T experience is highly desirable.Extensive experience … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal stakeholders ... Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and change… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director , US Pharma Payer Marketing Atherosclerosis leads a team of payer marketers dedicated to developing access strategies and tactics for a ... which is currently in Phase 3 Clinical Development. The Director will work closely with the US Commercial Leader...to the US Pharma Payer Marketing Lead as a member of the Payer Marketing leadership team and will… more
- Merck & Co. (Rahway, NJ)
- …Description: Corporate Card Strategy Lead The Corp Card Strategy Lead is an Associate Director role that sits within the Travel Meetings Card & ... Sourcing and Operations Team.- The role reports to the Director , Payments Services Sourcing and Strategy and is responsible...the following:Strategy Development: The role is a core team member of the Payments team and is responsible for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …a fast-paced environment. Relationships This position will report to the Associate Director , Strategic Market Intelligence. Working relationships with pipeline ... maximize your potential with us? The Position As a member of the Strategic Market Intelligence team, the primary...MBA, MSc or MPH preferred 5+ Years of relevant experience in sales analysis, forecasting, finance, pricing, or other… more
