- Takeda Pharmaceuticals (Boston, MA)
- …development of internal functional processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the ... processes and tools to enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Regional CPE Director , Tzield West/Mountains/South **Location:** Remote, US **About the job** **Role Overview:** The Regional Care Path Educator (CPE) ... Director will join the Type 1 Diabetes Commercial organization...and PCP/PED educational outreach efforts. We are an innovative global healthcare company with a focus on immunology that… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Regional Strategy and Account Director , Mid-Atlantic-Northeast **Location:** US Remote/Field **About the Job** The Regional Strategy and Account ... Director , Tzield will join the Type 1 Diabetes Commercial...account stakeholders are effectively engaged. We are an innovative global healthcare company with a focus on immunology that… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... for clinical deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical Program Quality… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …Oversee the process validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...+ Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies… more
- AbbVie (Boston, MA)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues.… more
- Takeda Pharmaceuticals (Boston, MA)
- …analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs . Advanced understanding in DMPK, ... with regulatory agencies. + Must have experience in global regulatory submission requirements and processes. **Program Leadership Skills/Competencies:**… more
- J&J Family of Companies (Cambridge, MA)
- …of internal and external human data resources. + Partner with Clinical Development, Global Regulatory Affairs , Data Science, Patient Reported Outcomes, ... while championing patients every step of the way. We are searching for a ** Director , Computational Multiomics, Neuroscience,** to be located at one of our offices in… more
- Takeda Pharmaceuticals (Lexington, MA)
- …"escalated" cases from the Medical Information Contact Center. + Represent US Medical Affairs at Global Core Response Document meetings with authority to approve ... the US Medical team, you will report to the Director , US Medical Information and Review. This is a.../ clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial… more
- Wolters Kluwer (Boston, MA)
- …Relationship Manager** will be calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs , Directors of Medical Affairs , ... dates, based on customer needs + Provide accurate weekly forecast updates to Director of Sales + Regular travel within territory and required customer facing… more