- Gilead Sciences, Inc. (Oceanside, CA)
- …to cross-functional teams, including Manufacturing, Quality Assurance, Process Development, and Regulatory Affairs . + Participate in the development and ... action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the… more
- AbbVie (Irvine, CA)
- …supporting the overall product development plan based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... with those requirements. Provide clinical development expertise for key regulatory discussions. Accurately summarize and communicate complex scientific … more
- Ascendis Pharma (Princeton, NJ)
- …the US, Germany & Austria, with plans for rapid expansion. As our new Director of US Communications and Public Relations, you will be spearheading all communications ... will report directly to the Head of US Public Affairs and be based in Princeton, NJ. This opportunity...in the rare endocrine space and translating our core scientific platform into locally relevant engagements with key stakeholders.… more
- Amneal Pharmaceuticals (Bridgewater, NJ)
- …studies. + Work closely with cross-functional teams (R&D, clinical development, regulatory affairs , commercial) to ensure medical insights are integrated ... Director Oncology will serve as an internal scientific expert supporting Oncology, Biosimilars, Branded Oncology and GRx...strategy. This position will report to the VP- Medical Affairs Essential Functions: + Provide clinical and scientific… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …+ Leads GMA-driven evidence generation, taking into consideration the medical, scientific , regulatory and commercial considerations + Supports multi-disciplinary ... Patient Advocacy, Professional Meetings and Conferences, and regular HCP scientific exchange, etc. to deliver Takeda's scientific ...as a study Medical Lead for the GMA Medical Affairs Company Sponsored / Collaborative studies + Manages complex… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …to cross-functional teams, including Manufacturing, Quality Assurance, Process Development, and Regulatory Affairs . + Participate in the development of ... action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the… more
- Takeda Pharmaceuticals (Boston, MA)
- … regulatory requirements. Serve as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global Device Sub team (GDT) to ensure ... regulatory requirements and guidelines. - Knowledge of other relevant regional regulatory nuances and requirements. - Knowledge of scientific principles and … more
- Bristol Myers Squibb (San Diego, CA)
- …and optimize product benefit-risk profiles. The ED works cross-functionally with clinical, regulatory , medical affairs , quality, and commercial teams to support ... submissions + Cross-Functional Leadership and Stakeholder Engagement + Partner with clinical, regulatory , and medical affairs teams to integrate safety insights… more
- Houston Methodist (Houston, TX)
- The Director of Educational Partnerships plays a critical leadership role in planning, directing, and implementing education and training initiatives across ... graduate research programs within the Houston Methodist Academic Institute (HMAI). The Director ensures that all students and trainees are immersed in the… more
- Otsuka America Pharmaceutical Inc. (San Juan, PR)
- …as an clinical/medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who will be...following: + Consults with patients or their representatives, clinical, regulatory , and scientific leaders and thoughtfully applies… more