- Bristol Myers Squibb (Boston, MA)
- …experience working in a matrixed industrial environment. The Clinical Biomarker Asset Lead role will be responsible for development and execution of translational ... assigned programs. Key responsibilities of this role are to act as a lead scientist to implement and deliver on biomarker strategies for clinical programs, develop… more
- Bristol Myers Squibb (Cambridge, MA)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... plus incentive cash and stock opportunities (based on eligibility). For the Associate Director position, the starting compensation for this job is a range from… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …divisions (eg TGRD and TPNA/TPEU/TPC). Lead TGRD internal teams and may lead global cross-functional teams, as appropriate. + Hires, manages, mentors, ... + Therapeutic area knowledge relevant to mechanism of action + Regional/ global Regulatory requirements + Emerging research in designated therapeutic… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …R&D USBU; GPLS, JPBU). Lead R&D internal teams and may lead global cross-functional teams, as appropriate. **EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:** ... + Therapeutic area knowledge + Pulmonologist/Neurologist with sleep medicine expertise + Regional/ global Regulatory requirements + GCP/ICH + Emerging research in… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …matrix teams + Diplomacy and positive influencing abilities + Knowledge of regional/ global Regulatory requirements and GCP/ICH TRAVEL REQUIREMENTS: + Ability to ... empower you to shine? Join us as a Medical Director , Clinical Science, Neuroscience TAU- Respiratory/Sleep Disorder in our...the global strategy. + May act as Global Clinical Lead for an early or… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ **Quality Expertise** : Provide technical quality expertise in compliance with global regulatory requirements and internal policies for Product Development ... key quality liaison between Biologics Business Unit senior management and Global Quality, Regulatory Affairs, and Operations, fostering seamless communication… more
- Sanofi Group (Cambridge, MA)
- …with the Global Project Head, Research Scientist, Clinical Pharmacologist, Biomarker Lead , Safety Medical Director , Statistician, Regulatory and other ... **Job Title:** Clinical Research Director **Location:** Cambridge, MA, **About the Job** Are...Plan (RMP), etc. + Contribute to briefing packages for regulatory meetings. + Lead discussion at meetings… more
- Sumitomo Pharma (Boston, MA)
- …. The Director , Patient & HUB Operations, Rare Disease will lead the strategy, development, and operation of the RETHYMIC CONNECT(R) patient support program ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and experienced individual for the position of ** Director , Patient & HUB Operations, Rare Disease**… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and positive influencing abilities Knowledge + Gastroenterology area knowledge desired + Regional/ global Regulatory requirements + GCP/ICH **TRAVEL ... you to shine? Join us as an Executive Medical Director in our GI & Inflammation Therapeutic Area Unit.../ Clinical team membership + Leads clinical teams as Global Clinical Lead or represents Clinical Science… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **Associate Director , Global Insights and Demand Forecast Lead ** **Cambridge, MA or Bannockburn, IL** ... empower you to shine? Join us as an Associate Director of Global Insights and Demand Forecast....and discipline in the process, across the portfolio + Lead insight generation of global plasma industry… more