- Merck & Co. (Rahway, NJ)
- …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... Job DescriptionThe Associate Principal Scientist, General Medicine Publications Medical Writing,...publication agency partners within assigned therapeutic area(s)/product(s) to ensure quality and consistency (as needed) Ensure that information for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …or More Years in the pharmaceutical industry preferred1 or More Years in regulatory affairs requiredExperience in (s)NDA/BLA filing to FDA preferred Travel ... support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs . Has a positive approach to work projects and ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Expert understanding of the pharmaceutical industry including marketing, medical, access, public affairs , compliance, legal and regulatory as well as the ... collaborators, as we embark on shaping our future. The Position The Associate Director, HCP Experience has overall strategic and operational responsibility as well… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Affairs , Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs , ... efficient, adaptable, and scalable architectures in accordance with company policies, regulatory standards, and integration methodology. Work with the business users… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... Affairs , Marketing, Legal, Quality , and other affiliates. External stakeholders include Healthcare professionals, HAs, ECs, DMCs, and Academia. Line management of… more
- Englewood Lab, Inc (Totowa, NJ)
- Title: Regulatory Affairs Associate Reports to: Manager of Regulatory Affairs Department: Quality / Regulatory Responsibilities: + Assist the ... of the Head of Quality / Regulatory . + Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP… more
- Haleon (Warren, NJ)
- …projects. **What will your individual contribution at Haleon be?** The expectation for the Regulatory Affairs Associate role will be as follows: + Work ... goal. Right now, we're looking for Co-Ops student in Regulatory Affairs to join us to do...supply products that are of proven safety, efficacy and quality , and make a worthwhile contribution to public health… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly ... focus on Clinical Regulatory filings and provide regulatory leadership on...to ensure attainment of governmental approvals. + Responsible for quality and timeliness of IND/CTA and BLA submissions. Interact… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review… more
- Organon & Co. (Jersey City, NJ)
- …**The Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate ... scientists in the Organon franchise teams. + Lead development and execution of regulatory CMC strategies to ensure high quality , accuracy, and high likelihood… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
- System One (Florham Park, NJ)
- …(Hybrid 2-3 days onsite) 12-month contract (renewable) Overview The Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal ... Senior Manager, Regulatory Affairs (BRANDED PRODUCTS) Must be...regions, and provide insights to the Senior Director and Associate Director. + Contribute to managing regulatory … more
- Novo Nordisk (Plainsboro, NJ)
- …personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs . Has a positive approach to work projects and ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- CUNY (New York, NY)
- …administrative leaders. + Advanced experience and knowledge about healthcare compliance, regulatory affairs , and operations. + Knowledge of medical school ... Senior Associate Dean for Academic Affairs **POSITION...in the field of medicine and on training high quality , culturally competent health professionals and scientists equipped to… more
- Bristol Myers Squibb (Madison, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical, Multiple Myeloma will report to the Director, US ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will support the… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …creative approaches to the management of programs including accreditation and regulatory affairs , patient safety, risk management, utilization management, bed ... approximately 60,000 Veterans) is hiring for a Chief of Quality , Service, and Value (QSV). This position functions as...program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus… more
- Veterans Affairs, Veterans Health Administration (New York, NY)
- Summary The HRO Coordinator is a member of Quality Management reporting directly to the Chief. The HRO Coordinator is responsible for fostering the development of an ... intact and working together seamlessly. Open to current Department of Veteran Affairs employees Responsibilities Open to current Department of Veteran Affairs … more
- Veterans Affairs, Veterans Health Administration (New York, NY)
- …of performance include knowledge and active participation in the unit/program level quality improvement process and initiatives as well as customer service programs. ... of care. Coordination also includes assuring services interface within the Veterans Affairs (VA) and community programs to provide continuity of care to Veterans.… more
