- Daiichi Sankyo, Inc. (Bernards, NJ)
- …documents (eg SOPs) as appropriate.Collaborate with cross-functional teams (eg, Medical Safety , Regulatory Affairs , Epidemiology) to ensure benefit-risk ... optimize, and innovate signal detection and management processes across the global safety organization. The incumbent will ensure regulatory compliance, promote… more
- Merck & Co. (Rahway, NJ)
- …--Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5… more
- Merck & Co. (Rahway, NJ)
- …studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Clinical Director May Be… more
- Merck & Co. (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The role of Associate Director, Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Focusing on Dermatology, in this role, you will be responsible for establishing/continuing economic Modelling research… more
- Reckitt (Parsippany, NJ)
- Regulatory and Safety Affairs Associate City: Parsippany **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition ... to grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate , Regulatory and Compliance provides regulatory … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director, Global Regulatory Affairs , you will act as ... role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. Position will be filled in either Foster City,… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …please visit Gilead.com. We have an exciting opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical ... experience inOncologyMedicalAffairs + Industry experience with knowledge of all applicable regulatory and legal requirements for Medical Affairs activities +… more
- Merck (Rahway, NJ)
- …+ Proven track record in setting and delivering product strategy in regulatory affairs and pharmacovigilance domains, with an ability to execute ... regulatory authoring/publishing platforms. + Demonstrated experience delivering regulatory affairs and pharmacovigilance technology solutions (authoring/publishing,… more
- J&J Family of Companies (Raritan, NJ)
- …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... is preferred. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs , Clinical, Medical Information, Pharmacovigilance, etc.) is required.… more
- J&J Family of Companies (Raritan, NJ)
- …as Medical Affairs , Medical Safety , Post Market Surveillance, Clinical Affairs , Design Quality Engineers, R&D, and Regulatory Affairs relating to ... at https://www.jnj.com/medtech We are searching for the best talent for an ** Associate Director, Medical Writing & Literature Services** . _Remote work options may… more
- System One (Bridgewater, NJ)
- Title: Regulatory /QA Sr. Associate Type: Direct Hire Location: Morris County, NJ Hours: 9am-5pm (Hybrid schedule) . Must have: + Strong experience with product ... key role in maintaining and enhancing product quality and regulatory compliance. Reporting to the Associate Director...with internal quality standards + Balance customer satisfaction with regulatory and safety compliance + Manage risk… more
- Ascendis Pharma (Princeton, NJ)
- … Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA safety ... for employees to grow and develop their skills. The Associate Director, ICSR Management Team reports to the Director,... regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to 20%… more
- AbbVie (Florham Park, NJ)
- …of work may include clinical trials, patient safety , and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , and GMA, etc.) to create development… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical Neuropsychiatry position works in the US Medical ... points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical Neuropsychiatry.… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5 more}… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more
