- J&J Family of Companies (Trenton, NJ)
- Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a highly experienced … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …the best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing...US based employees may be eligible to participate in medical , dental, vision insurance, a 401(k) plan and company… more
- Merck (North Wales, PA)
- …diagnostic regulations on the development and registration activities for the respective medical products. + Providing regulatory support for due diligence ... **Job Description** Our Diagnostics focused Regulatory Affairs team helps bring new precision medicine advancements to the world by facilitating effective,… more
- Bristol Myers Squibb (Princeton, NJ)
- …external resources; ensure appropriate quality controls in place for compliant submissions + Writing regulatory documents (eg new INDs, briefing book content, BT ... careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development and through life… more
- J&J Family of Companies (Horsham, PA)
- Medical Director , Gastroenterology Therapeutic Area - Medical Affairs - 2406204236W **Description** Johnson and Johnson is recruiting for a Medical ... and executing the US Gastroenterology TA strategic plan for Medical Affairs. The Medical Director ,...in Gastroenterology TA and other groups inside and outside Medical Affairs (eg Biostats, GCO, Regulatory Affairs,… more
- Integra LifeSciences (Princeton, NJ)
- …challenging what's possible and making headway to help improve outcomes. The ** Director of Post Market Surveillance** is responsible for developing, directing and ... and Post Market Surveillance activities required for EU MDR and other global regulatory bodies. This role will establish a Post Market Surveillance program that… more
- Merck (Philadelphia, PA)
- **Job Description** **Position Description:** **Associate Director , Policy Advocacy** The Associate Director , Policy Advocacy serves as the senior expert in the ... policy change in support of the company's business objectives. The Associate Director will proactively research and stay abreast of new strategies and tactics… more
- J&J Family of Companies (Titusville, NJ)
- …Global Development (clinical trial startup, performance, oversight, and results reporting), Medical Writing (document templates and clean authoring), Therapeutic ... At least 10 years' of relevant pharmaceutical/scientific experience (in clinical development or medical writing preferably) + At least 10 years' of people… more
- Merck (Philadelphia, PA)
- …think tanks, or business associations responsible for healthcare, commercial trade, regulatory , or intellectual property + Pharmaceutical sector, medical device, ... **Job Description** **Position Description:** **Associate Director , Policy Strategy and Capabilities** The Associate Director , Policy Strategy and Capabilities… more
- University of Pennsylvania (Philadelphia, PA)
- …In collaboration with Principal Investigators and the FTDC Clinical Research Program Director , the Regulatory Project Manager will take a leadership role ... in writing , submitting, implementing and continued management of investigator-initiated protocols....Director . Job Description Job Responsibilities + Independently manage regulatory needs of clinical and non-clinical trials and studies… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Director , Clinical Research Operations (Department of Dermatology) Job Profile Title Director ... alignment with the University of Pennsylvania, GCP, FDA and all applicable regulatory bodies. The candidate must have a comprehensive understanding of clinical trial… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Research Project Director Job Profile Title Manager Research Project C Job Description Summary The ... phenomena at both the basic and applied levels. The Lab is led by Director Dolores Albarracin, Ph.D., the Alexandra Heyman Nash University Professor, and the 28th… more
- Taiho Oncology (Princeton, NJ)
- …execution, analysis and reporting of data, and authoring/review of scientific and regulatory documents. The Director , Biostatistics will have responsibility for ... Director , Biostatistics Princeton, NJ, USA Req #391 Thursday,...clinical data. + Creates/authors statistical sections of scientific and/or regulatory documents, eg-IND etc. + Represents and defends protocol… more
- Marriott (Trenton, NJ)
- …**Position Type** Management **JOB SUMMARY** Marriott has an exciting opportunity for a Director on the Corporate Systems team within the Finance domain. This role ... owning technology and supporting Marriott's critical enterprise applications. The Director , Financial Systems will lead the strategic design, implementation, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director will be responsible for supporting the development and ... for the management of the program and will report directly to the Director , Patient Access & Support Services. This individual will be responsible for creating… more
- J&J Family of Companies (Titusville, NJ)
- …experience. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at ... Associate Director , RA Labeling Product Leader (1 of 2) -...least 6 years of direct regulatory labeling content experience developing and writing labeling… more
- Taiho Oncology (Princeton, NJ)
- …of internal disciplines such as clinical operations, data management, Pharmacovigilance Operations, Medical Writing and Regulatory Affairs is a plus. ... Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA...negotiation, and project award. + Ensure compliance with all regulatory and reporting requirements related to Supplier Diversity and… more
- Integra LifeSciences (Princeton, NJ)
- …and making headway to help improve outcomes. **SUMMARY DESCRIPTION** The Director , Service & Repair and Quality Distribution directs, coordinates, and evaluates ... and policies that ensure the development, manufacturing, distribution, and S&R of medical devices in compliance with corporate policies, US Food and Drug… more
- Bristol Myers Squibb (Princeton, NJ)
- …be a credible interface to all global development and business partners ( medical , development, commercial, regulatory , quality etc.). + Influential leadership ... for clinical trial data acquisition, data standards governance, data management, medical coding, data reporting and analytics, and centralized monitoring for trials… more
- West Pharmaceutical Services (Trenton, NJ)
- …with a good technical understanding and knowledge of combination products, medical device qualification, primary packaging, regulatory requirements, and program ... Director , Business Development for Drug Packaging and Delivery...candidate will have a strong background in pharmaceuticals and medical device, with a deep understanding of drug delivery… more