- 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 (Trenton, 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
- 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
- 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
- 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
- Publicis Groupe (Philadelphia, PA)
- …and career development + Provide estimates for SOW development + Work with the Director , Regulatory Review in the development of departmental SOPs + Oversee work ... www.digitashealth.com | Facebook: www.facebook.com/digitashealth| Twitter: www.twitter.com/digitas_health **Overview** The Manager, Regulatory Review is responsible for managing a team of… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …writing strategy for key clinical and regulatory documents and regulatory submissions; guides medical writing document preparation, including ... Writing team, you will report to the Associate Director . **How you will contribute:** + Reporting to a...Principal Medical Writer guides medical writing activities for key clinical and regulatory … more
- J&J Family of Companies (Spring House, PA)
- …such as nonclinical safety, pharmacokinetic, and discovery biology project leaders, medical writers, global regulatory dossier leaders, and other subject ... Skills:** **Required:** + Experience working globally as lead author on writing Toxicology, Pharmacology, Pharmacokinetics, or Bioanalytical regulatory documents… more
- J&J Family of Companies (Titusville, NJ)
- …2 years of Medical Information or strong clinical practice experience * Medical writing experience and proven ability to conduct literature analysis. * ... Manager, Medical Information Scientific Engagement (MISE) - Titusville, NJ... Information Scientific Engagement (MISE) reports to the Associate Director MISE and is responsible for engaging healthcare professionals… more
- University of Pennsylvania (Philadelphia, PA)
- …Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work closely with ... of the team's work, working closely with the CRU Regulatory coordinators to manage, review and initiate trials to...The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's, report… more