- Takeda Pharmaceuticals (Cambridge, MA)
- …Description** **OBJECTIVES:** + Leads flagships medical programs as defined by the Global Medical Affairs (GMA) Strategy Team and sub-teams + Leads GMA-driven ... evidence generation, taking into consideration the medical, scientific, regulatory and commercial considerations + Supports multi-disciplinary matrix teams through… 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)
- …+ 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 (Lexington, MA)
- …This role serves as the key quality liaison between Biologics Business Unit senior management and Global Quality, Regulatory Affairs, and Operations, ... + **Quality Expertise** : Provide technical quality expertise in compliance with global regulatory requirements and internal policies for Product Development… 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
- 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 ... will plan, direct, and coordinate specialized and complex global development projects led by the Rheumatology group within...submissions. + Provide input to the Statistics Group Lead ( Senior Director or Executive Director )… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director /Principal Medical Writer **Location:** Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the future of ... and Project Team. This is a position for a senior medical writer who has an extensive experience with...extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as submission… more
- Amentum (Boston, MA)
- …and other business units on risk-related initiatives. + Serve as a deputy to the Senior Director and provide mentorship to the risk management team. + Represent ... seeks a Director , Insurance and Risk Management.** **Amentum** is a global leader in advanced engineering and innovative technology solutions, trusted by the… more
- Hologic (Marlborough, MA)
- …Audit Program, ensuring compliance with FDA regulations, ISO standards, and other global regulatory requirements. If you thrive in a fast-paced, collaborative ... Director , Internal Audit Marlborough, MA, United States Are...standards (eg, ISO 13485:2016, ISO 14971), MDSAP, and other global regulatory requirements. + Expertise in Quality… more