- J&J Family of Companies (Spring House, PA)
- 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)
- … response documents and key components of regulatory submissions. + The Associate Director , Medical Writing is seen as an expert in medical ... therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you...documents. Collaborate with all Takeda regions to ensure a medical writing regulatory document strategy… 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
- J&J Family of Companies (Horsham, PA)
- Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory ... Authorities. + Provides technical expertise and technical input in the preparation and writing (as applicable) of regulatory dossiers for submission to Health… more
- J&J Family of Companies (Titusville, NJ)
- … safety, biostatistics, regulatory affairs, clinical supplies unit, medical writing , clinical pharmacology, legal, finance, quality assurance, strategy ... Medical Director , Clinical Development - Psychosis... Regulatory Affairs in the development of drug regulatory strategies + Executes medical -related consultation for… more
- Organon & Co. (Plymouth Meeting, PA)
- …support the approved early development plans. The TMED Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction ... **The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible for… more
- Penn Medicine (Philadelphia, PA)
- …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... Blvd. Philadelphia, PA** **Hours: 8hr Days (HYBRID)** **Summary** : + **The Director of Health Justice Transformation** is a unique opportunity to help establish… more
- Cardinal Health (Trenton, NJ)
- …(CMC) Development + Nonclinical Development and Consulting + Clinical Development and Research + Medical Writing + Regulatory Publishing + Dossier Services + ... & Filing + Quality Review Standards + Drug, Biologic (IV, Injectable) and Medical Device Development + Regulatory Outsourcing + Pharmaceutical Compliance + … more
- Fujifilm (Trenton, NJ)
- **Overview** As the Associate Director of Biosafety, you will serve as the Corporate Biosafety Officer (BSO) and provide expertise in biorisk management, ... and safety. This position will report to the Global Director , Biosafety and Toxicology, and sit under the global...Toxicology, and sit under the global quality leadership group ( Regulatory , IT, Safety, QA, and QC). **External US** The… 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
- 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
- Bristol Myers Squibb (Princeton, NJ)
- …be a credible interface to all global development and business partners ( medical , development, commercial, regulatory & quality etc.). + Influential leadership ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership role with oversight to… more
- Bristol Myers Squibb (Princeton, NJ)
- …design. Develops study designs that address study objectives that will support regulatory approval, medical research and market access. + Independently leads, ... in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Director of Biostatistics is a member of cross-functional team and… more
- Merck (North Wales, PA)
- …lead clinical scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical/scientific and regulatory documents. + Partners with Study ... of clinical data/ medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities of direct and indirect team members… 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
- Genesis Healthcare (Langhorne, PA)
- …pay classification, job grade, location, and length of service. The Assistant Recreation Director is responsible for assisting the Recreation Director in the ... to the development of program philosophies and policies, along with writing procedures, goals and objectives for the program.*Contribute to the implementation… more
- Organon & Co. (Plymouth Meeting, PA)
- …promotional regulatory strategy in collaboration with Commercial, PRT, Global Regulatory Liaisons, Medical Affairs and Worldwide Product Labeling. + Guide ... writing ability, effective communication and familiarity with worldwide regulatory agencies. + Experienced in negotiations with health authorities. + Outstanding… more
- Bank of America (Pennington, NJ)
- Sr Quantitative Finance Analyst (VP/ Director ) - Liquidity Model Validation Charlotte, North Carolina;Pennington, New Jersey; Atlanta, Georgia **Job Description:** At ... in the Bank. Responsible for compliance with Enhanced Prudential Standards and other regulatory guidelines, the candidate will work on models related to both banking… more