- Sanofi Group (Waltham, MA)
- …development, submission, launch and life cycle management of a medium vaccine project (5-7 clinical studies and global submission in key markets) or, a major ... **Job Title:** Senior Project Biostatistics Lead - Vaccines **Location:** Waltham, MA **About the Job**...The incumbent is accountable for all statistical aspects of clinical development/medical affairs plans, studies and submissions… more
- Bristol Myers Squibb (Cambridge, MA)
- …training Clinical Development Expertise & Strategy + In collaboration with the Clinical Development Lead , designs and develops clinical plans and ... targets + Provides oversight and medical accountability for a group of studies + Leads the analysis...reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …+ Provides scientific and strategic leadership as the Global or Regional Clinical Pharmacology Lead for multiple projects on Global Program Teams ... people and the planet. Our Data and Quantitative Sciences group (DQS) is made up of more than 500...knowledge and experience with design, analysis, and reporting of clinical pharmacology studies . + Specialized clinical… more
- Sumitomo Pharma (Boston, MA)
- …**Job Duties and Responsibilities** + Responsible for and lead all activities related to clinical study design from clinical study concept to ... highly complex decisions + Leads and drives strategy for clinical studies for assigned asset(s) within the... clinical trial results and the writing of clinical study reports + Contributes to the… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as Director, Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. Our Data and ... + Provides scientific and strategic leadership as the Global or Regional Clinical Pharmacology Lead for multiple projects on Global Program Teams… more
- Sanofi Group (Cambridge, MA)
- …in the TA, including clinical development plans, protocols, primary data read-outs, clinical study reports and primary publications. + Be a key thought ... thought was possible. Ready to get started? **Main Responsibilities:** + Lead the clinical development organization within the immunology TA (over 50 physicians… more
- Sumitomo Pharma (Boston, MA)
- …director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators ... and study staff. + Responsible for leading clinical study teams, monitoring overall study...regulatory, and legal standards. + May participate in or lead clinical development contributions to due diligence… more
- Merck (Boston, MA)
- …the activities of Clinical Scientists in the execution of clinical studies . + Work closely with a cross-functional group of experts in commercialization, ... trials for investigational drugs + Analyzing and summarizing the clinical findings from studies to support decisions...safety and efficacy as well as new drug applications, clinical study reports, or publication; and +… more
- Sanofi Group (Cambridge, MA)
- …Project Leader: + oversee the efforts in setting, conducting and closing clinical studies , ensuring everything runs smoothly and efficiently. + defining ... trials operations + Develop the operation plan + lead the cross-function study team and oversee...expansion + any complex design + Familiar with all pre- clinical activities (eg Toxicity studies ) + Collaborates… more
- Sanofi Group (Cambridge, MA)
- …A summary of responsibilities include: + Lead the strategy of global medical- lead studies for Tolebrutinib, including the management of the study ... disorders around the world. Reporting to the Global Medical Lead for Tolebrutinib, the Global Senior Medical Director for...will oversee all data generation activities (phase IV interventional studies , RWE studies , ESR) for Tolebrutinib, from… more