- J&J Family of Companies (Skillman, NJ)
- Senior Associate , Regulatory Affairs - 2407025090W **Description** Kenvue is currently recruiting for: Senior Associate , Regulatory Affairs , ... **Travel %:** <10% **Pay: 84k- 152k** **What you will do** The Senior Associate , Regulatory Affairs is responsible for developing regulatory strategy and… more
- Taiho Oncology (Princeton, NJ)
- Associate Director, Regulatory Affairs Operations Pleasanton, CA, USA * Princeton, NJ, USA Req #386 Tuesday, August 20, 2024 Looking for a chance to make a ... our dynamic and expanding mid-size oncology company in the role of Associate Director, Regulatory Affairs Operations where you will utilize your knowledge… more
- Globus Medical, Inc. (Audubon, PA)
- …so patients can resume their lives as quickly as possible. **Position Summary:** The Regulatory Affairs Associate assists in drafting, submitting and gaining ... in medical device industry or equivalent, preferably within orthopedic medical devices; Regulatory Affairs experience is a plus + Excellent communication and… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for ... labeling, and for coordinating internal labelling activities and processes for regulatory submissions and product maintenance. The Associate Director prioritizes… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …from Veeva PromoMats on job volume and overall PRC performance. + Perform other regulatory tasks as assigned. **Requirements:** + Bachelor's Degree + Minimum 1 to 2 ... position, with or without reasonable accommodation. **Key Stakeholder Relationships** Regulatory , Legal/Compliance, Medical, Marketing, Creative Agencies Intra-Cellular Therapies is… more
- Bausch Health (Bridgewater, NJ)
- …and procedures to enhance efficiencies and compliance. + Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess and ... and promotion review experience. Broad knowledge of the pharmaceutical industry Regulatory Affairs discipline for prescription drugs. + Detail-oriented with… more
- Bristol Myers Squibb (Princeton, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
- Merck (North Wales, PA)
- …Director/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Novo Nordisk (Princeton, NJ)
- …designated personnel. Relationships Report to the Director/ Associate Director/Lead Regulatory Scientist/Sr. Manager Regulatory Affairs . Develop and ... maintain positive rapport and working relationships with other personnel in Regulatory Affairs , CMR, and other local and headquarter departments to accomplish… more
- Bausch + Lomb (Bridgewater, NJ)
- …transfers and geographical expansion projects on behalf of the Global Regulatory Affairs department. **Responsibilities** * Responsible for general knowledge ... degree, Bachelor degree preferred or equivalent * Minimum 1.5 years of Regulatory Affairs Project management experience * PMP Certification preferred Specific… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global ... changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global Regulatory Project Management… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …FDA/EMA/PMDA regulations; ICH guidance; GLP/GCP requirements; SEND requirements, etc.). + Regulatory Affairs Credential (RAC-Drugs) is an advantage. + Strong ... to the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology… more
- Bristol Myers Squibb (Princeton, NJ)
- …MS or commensurate experience preferred **Experience Requirements** Significant experience in regulatory affairs (eg 3-5 years) **Key Competency Requirements** ... careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development and through life… more
- Catalent Pharma Solutions (Somerset, NJ)
- …NJ is hiring a Senior Regulatory and Compliance Specialist for the Regulatory Affairs Group. The Senior Regulatory and Compliance Specialist candidate ... organization as it touches various functional areas including: Supplier Quality, Regulatory Compliance, DEA, and Quality Management Systems. This role is part… more
- University of Pennsylvania (Philadelphia, PA)
- …resources, and much more. Posted Job Title Quality Assurance Specialist ( Regulatory ) CVPF(Center for Cellular Immunotherapy) Job Profile Title Research Coordinator ... to help with raw materials release, new hire QA Associate train. Position contingent upon funding. Qualifications + Bachelor...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director, Medical Excellence and Impact - 2406214789W **Description** Johnson and Johnson Family is recruiting an ** Associate Director, Medical** ... of the disease. **Position Overview:** We are seeking a dynamic and forward-thinking Associate Director, Medical Excellence Lead to join our team. This role is… more
- Bristol Myers Squibb (Princeton, NJ)
- …partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory , IT, Audit, Finance and HR to build and integrate one global ... Responsibilities Include : + Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data… more
- J&J Family of Companies (Horsham, PA)
- Associate Director, MSL Communications - Immunology - 2406205683W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate Director, ... impact health for humanity. Learn more at https://www.jnj.com/ . The Associate Director, Medical Science Liaison (MSL) Communications, will be responsible for… more
- J&J Family of Companies (Horsham, PA)
- Associate Director, Real World Value and Evidence - Hematology - 2406214039W **Description** Johnson & Johnson is currently recruiting an Associate Director, ... humanity. Learn more at https://www.jnj.com/. In this in-house position, the Associate Director, RWV&E, will be responsible for conducting real-world evidence… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …bipolar depression in adults as monotherapy and as adjunctive therapy. ** Associate Director/Director, Data Management** will oversee and provide guidance (both ... trials. + Provide direction to study team to maximize compliance with regulatory requirements; review and suggest improvements to operating procedures and policies… more