- Novo Nordisk Inc. (Plainsboro, NJ)
- …on digital channels Manages and builds relationships with internal teams; Legal, Medical and Regulatory Translates best practices for digital and corporate ... change lives for the better. The Position The Associate Director , Digital Content Strategy & Production reports to the...ability to jump from creative to analytics Maintains excellent writing and language skills Enjoys a working knowledge of… more
- 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)
- … 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 (Titusville, NJ)
- 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
- Novo Nordisk (Plainsboro, NJ)
- …Disease department. Work with the Clinical Operations, Non-Clinical Research, Medical Writing , Program Management, CMC and Regulatory Affairs teams. Will be ... ready to make a difference? The Position The International Medical Director serves as a subject matter...Work with, Clinical Operations, Non-Clinical Research, Medical Writing , Program Management, CMC and Regulatory Affairs… 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
- Olympus Corporation of the Americas (Center Valley, PA)
- …**__** Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can ... other than @Olympus.com, it is likely not legitimate._ **Job Description** The Director Scientific Communications, Global Operations plays a central role in the… 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
- Pfizer (Collegeville, PA)
- …with very complex but different distribution and provider cost recovery dynamics. The Director , Contract Strategy & Modeling is a key member of the Oncology ... hospital systems, GPO customer segments and key accounts. The Director Contract Strategy & Modeling reports directly to the...on getting things done quickly and simply + Excellent writing , oral and presentation skills; Ability to convey 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
- Novo Nordisk (Plainsboro, NJ)
- …on digital channels + Manages and builds relationships with internal teams; Legal, Medical and Regulatory + Translates best practices for digital and corporate ... change lives for the better. The Position The Associate Director , Digital Content Strategy & Production reports to the...to jump from creative to analytics + Maintains excellent writing and language skills + Enjoys a working knowledge… more
