- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...and GCP guidelines as well as applicable SOPs regarding clinical safety + Possesses proficient scientific expertise… more
- Actalent (Paramus, NJ)
- MUST BE ON-SITE IN PARAMUS, NJ 5 DAYS/WEEK The Associate Director , Clinical Operations is responsible for oversight of US clinical development providing ... clinical trial implementation, execution, and outcome, building consensus within the global clinical operations team. The Associate Director is also… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Clinical Scientist leads in the development, evaluation, planning and execution of hematology oncology clinical studies and ... on clinical studies and programs. May be responsible to manage one or more clinical scientists. As an Associate Director , a typical day may include the… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Clinical Project...day to day management of one or more global clinical studies, in compliance with department safety ... Scientist - 2406187180W **Description** Johnson & Johnson is currently seeking an Associate Director , Clinical Project Scientist to join the Oncology Global… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Clinical Operations Pleasanton, CA, USA * Princeton, NJ, USA Req #367 Wednesday, May 8, 2024 Looking for a chance to make a meaningful ... and manages multiple complex global studies to support the Clinical Development Plan. The Associate Director...procedures and oversees the quality of the data and safety of the patients. Communicates deviations from the protocol,… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Pleasanton, CA, USA * Princeton, NJ, USA Req #361 Monday, April 22, 2024 Looking for a chance to make a meaningful difference in ... Value Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance… more
- The Mount Sinai Health System (NJ)
- …the Icahn School of Medicine at Mount Sinai is actively recruiting an Associate Program Director for Internal Medicine Residency.** Valley Health System (VHS) ... Medicine at Mount Sinai (ISMMS) is actively recruiting an Associate Program Director for the newly accredited...for the IM continuity clinic. In addition to excellent clinical and leadership skills, the ideal candidate will have… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Scientific Associate Director , DMPK Project Representative** Challenging. Meaningful. ... drug-interaction potential of drug candidates. Working closely with drug safety and clinical pharmacology, Dev DMPK plays...across the globe. PCO is looking for a Scientific Associate Director to join the Dev DMPK… more
- Catalent Pharma Solutions (Hillside, NJ)
- ** Associate Director , Regulatory Affairs** **Position Summary:** Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical ... through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The...consumer and Catalent employee. The primary duty of the ** Associate Director , Regulatory Affairs** is to support… more
- Bristol Myers Squibb (Princeton, NJ)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing ... support of BMS medicines and all phases of associated clinical trials. The RAD oversees their regional team to...timelines + Contributes to managing external communication when significant safety issues arise, with the well-being of patients being… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. **Summary** The Associate Director , External Data Management, is accountable for the ... of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , Worldwide Oncology Communications, Corporate Affairs The ... Associate Director will be an integral member of the Worldwide...engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the… more
- Bristol Myers Squibb (Princeton, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, study results… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders. **SUMMARY** + The Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, and ... + Assess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease to characterize… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director Regulatory Process Development - 2406185269W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare ... https://www.jnj.com/. **Johnson & Johnson Innovative Medicine, is recruiting for an Associate Director , Regulatory Process Development (RPD).** The position can… more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The role of Associate Director of US Commercial Regulatory Affairs requires the ... institutional campaigns. + Proven aptitude to analyze and interpret efficacy and safety data. + Experience communicating and negotiating with OPDP/APLB is a plus.… more
- Bristol Myers Squibb (Princeton, NJ)
- …efforts. QSP modeling has become an important component of discovery and clinical development. QSP models are mechanistic, mathematical models, based on integration ... of non- clinical / clinical knowledge and data to represent varying...engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs, ... perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory...effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis - Develop and maintain necessary… more
- Novo Nordisk (Plainsboro, NJ)
- …while innovating for future capabilities. We regulate accounting, uphold workplace safety , manage our supply chain and sampling, support technology, provide ... independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships include… more
- Bristol Myers Squibb (Princeton, NJ)
- …in partnership with cross-functional Business Process Owners (eg Biostatistics, Regulatory, Clinical Development, Safety and Clinical Trial operations). ... required (six sigma training is a plus); within Drug Development ( Clinical Development, Trial Operations, Biostatistics, Regulatory, Safety , Project Management,… more