- Bristol Myers Squibb (Princeton, NJ)
- …skills and be capable of distilling the essential elements of complex issues for senior internal and external stakeholders and scientific and non- scientific ... with oncology asset level matrix teams, including market access, clinical development, medical affairs, regulatory, biostatistics to ensure full alignment… more
- Merck (Rahway, NJ)
- …We are currently seeking a Cardiovascular & Respiratory Competitive Intelligence Director specializing in PAH, COPD, and other cardiopulmonary diseases. This role ... insights, benchmarking, and recommendations for commercialization strategies, portfolio prioritization, clinical development/research strategies, and Business Development initiatives. + Partnering… more
- Bristol Myers Squibb (Princeton, NJ)
- … stakeholders, and operate effectively across global functions + **Skills:** + Strong scientific and analytical thinking applied in a clinical trial context + ... Read more: careers.bms.com/working-with-us . **Position Summary** The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Director , GxP Training Lead, is a senior leader within the Learning Center of Excellence under Global Quality. This role is responsible for developing and ... GxP training programs for all regulated functions (eg, R&D, Manufacturing, Clinical , Quality). + Implement innovative learning solutions leveraging adult learning… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... regulatory affairs, quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …competitor labeling - understanding precedents & opportunities. + Ability to assimilate key clinical , scientific , and medical information and present it in a ... efficient manner to meet required timelines. + Develop clear communications for senior management and SOP approvers to streamline and facilitate final label… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Director , Value and Access - PEDs-TDAP-Meningitis- Vaccines **Location:** Morristown, NJ **About the Job** Sanofi is seeking a strategic leader to ... : Collaborate with Pricing, Contracting, and HEVA teams to communicate the clinical and real-world value of therapies. Support field teams with strategic messaging… more
- GRAIL (Trenton, NJ)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... manage and provide direction to regulatory staff and, when required, participate in senior management meetings as a delegate. The role fosters a work culture aligned… more
- Merck (Rahway, NJ)
- …manufacturing to manage clinical development projects + Assist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead ... **Job Description** The ** Clinical Director (Principal Scientist)** has primary...to his/her areas of responsibility. **The Clinical Director is responsible for maintaining a strong scientific… more