- 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 ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... research areas centered around rare diseases and immune disorders.Summary The Associate Director, Global Clinical Operations (GCO) Procedural Ownership and Life… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …reasonable accommodation. Education Qualifications (from an accredited college or university)PhD in Life Sciences or in related discipline preferredMS degree in ... medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of...Life Sciences or in related discipline required ExperienceMinimum 3 years… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …(from an accredited college or university)Bachelor's Degree bachelor's degree in computer science , Life Science , Engineering, Business Administration or ... medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of...Qualifications7 or More Years Minimum 7 years' experience in life sciences , pharma with Clinical Trials Operational… more
- Aequor (Thousand Oaks, CA)
- …or pharmaceutical industry OR Associate 's degree and 6 years of Life Science or Business experience preferably in the biotechnology or pharmaceutical ... industry Associate 's degree and 6 years of Life Science or Business experience preferably in...a fluid environment with time pressures General understanding of regulatory guidelines impacting supply (ie GxP, SOX) High attention… more
- Merck & Co. (North Wales, PA)
- …+ 2 years Pharmaceutical and/or-clinical drug development experience. Degree in life sciences , preferred.NOTICE FOR INTERNAL APPLICANTSIn accordance with ... trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the… more
- Catalent (St. Petersburg, FL)
- QC Associate Scientist IIThe QC Associate Scientist II supports testing and release of raw materials, intermediate and finished products, and all critical ... specifications, standard operating procedures, approved test methods and/or protocols, regulatory requirements, and St. Petersburg's Quality departmental policies.II. Basic… more
- Insmed Incorporated (San Diego, CA)
- …development programs for products in a global, matrix organization, from Research to life cycle management. Additionally, the Associate Director of PM will work ... in the biopharma industry, come to Insmed to accelerate your career.RecognitionsNamed Science 's Top Employer in 2021, 2022, and 2023Insmed is dedicated to creating… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Education Qualifications (from an accredited college or university)Bachelor's Degree in life sciences or related field required Experience Qualifications 7 ... opportunity employer including veterans and people with disabilities. Summary The Associate Director, Clinical Data Standards, is responsible for the development,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …(from an accredited college or university)- Bachelor's Degree (preferred in Life Sciences ) with relevant clinical development experience requiredExperience ... medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of...the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Education Qualifications (from an accredited college or university)- Bachelor's Degree Life Science Degree required- Master's Degree preferred- PharmD preferred ... other research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC, is responsible for the regulatory CMC (Chemistry,… more
- Merck & Co. (Rahway, NJ)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... therapeutic areas and modalities to drive portfolio impact from discovery through life -cycle management. The team is externally visible and continues to be at… more
- Merck & Co. (Rahway, NJ)
- …fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the ... Text, Ethernet/Networking, and Analog/Metrology, to enhance process control systems.Utilize data science and data processing tools to analyze and interpret data for… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …accommodation.Education Qualifications (from an accredited college or university)Bachelor's Degree in a Life Sciences field and a minimum of 7 years of ... medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of...timelines and that quality of data is suitable for regulatory submission. The Associate Director will have… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …experience for degree 5+ years of experience including brand management/marketing experience, life science or related field Experience within the pharmaceutical ... to experiment with us? The Position The Consumer CX Associate will support the successful execution of brand/therapy area...or life science industry preferred Consumer marketing experience… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …college or university)- Bachelor's Degree required- Master's Degree Business Administration or Life Sciences preferred Experience- 7 or More Years Outsourcing, ... diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of scientific expertise and… more
- Novo Nordisk Inc. (WA)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... and cross-functional team in support of benefit risk profile throughout product life cycle. Collaborates with the PSL(s) to proactively plan and prioritize safety… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an accredited college or university required- Master's Degree Master's degree in Life Science or Engineering or Information Technology preferred Experience- 4 ... or More Years 4-7 Years of experience in applications development and business analysis in life sciences , pharma or informatics industry- 4 or More Years 4 or… more
- Eisai, Inc (Nutley, NJ)
- …tools: Microsoft Project, MS Visio, Tableau, and Data Priviledge; System development life cycles with GCP and related Regulatory guidelines; and, Programming ... technologies. Requires: Bachelor's degree or foreign equivalent in Computer Science , Technology, Electronics and Communication Engineering, or Business Intelligence… more
