- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... analysis plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide technical expertise and guidance on… 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 ... inspire you and empower you to shine? Join us as a Medical Director , Clinical Science, Neuroscience TAU- Respiratory/Sleep Disorder in our Cambridge, MA office. At… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to mechanism of action . Preferably with expertise Neurology or Psychiatry . Regional/ global Regulatory requirements . GCP/ICH . Emerging research in designated ... Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …+ Therapeutic area knowledge relevant to mechanism of action + Regional/ global Regulatory requirements + Emerging research in designated therapeutic ... Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …+ Therapeutic area knowledge + Pulmonologist/Neurologist with sleep medicine expertise + Regional/ global Regulatory requirements + GCP/ICH + Emerging research in ... Medical Director leads and drives strategy for the overall global (US/EU/Japan/China) clinical development taking into consideration the medical, scientific, … 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...realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation,… more
- Sanofi Group (Cambridge, MA)
- …diagnostic products within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within ... **Job Title:** GRA Device Lead ( Director ) **Location** : Morristown, NJ, Cambridge, MA, Framingham,...Global Research and Development. Sanofi's global regulatory affairs (GRA) function is comprised… 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
- Takeda Pharmaceuticals (Boston, MA)
- …or a related specialty, disease mechanisms and plasma derived/related therapies + Regional/ global Regulatory requirements + GCP/ICH + Emerging research in plasma ... empower you to shine? Join us as a Medical Director , Clinical Sciences - Plasma Derived Therapies in our...realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation,… more
- Pfizer (Cambridge, MA)
- …data management, result interpretation, and providing statistical support and leadership in global regulatory submission activities, as well as implementing new ... **JOB SUMMARY** The Director will plan, direct, and coordinate specialized and complex global development projects led by the Rheumatology group within the… more