- Takeda Pharmaceuticals (Cambridge, MA)
- …and policies. + Collaborate with internal cross-functional stakeholders (Marketing, PRT, Medical Affairs , Legal, Regulatory , Ethics & Compliance) to ensure the ... to the best of my knowledge. **Job Description** **About the role:** The Associate Director, Commercial Engagements & P2P Strategy, offers a unique opportunity to… more
- J&J Family of Companies (Danvers, MA)
- …America **Job Description:** **We are searching for the best talent for Associate ** **Director, Professional Education - Operations to join our Heart Recovery ... and do not limit your application. Purpose: We are seeking an ** Associate ** **Director, Professional Education - Operations,** who will be responsible for overseeing… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …chemistry, analytical development, drug product development, manufacturing, quality assurance, and regulatory affairs , to develop and implement effective process ... multiple projects, drive technical/scientific strategy and mentor junior engineers. The Associate Engineering Fellow will be leading complex programs and will be… more
- AbbVie (Boston, MA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. + May serve… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the ... for clinical deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical Program Quality… more
- Takeda Pharmaceuticals (Boston, MA)
- …processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation and change management ... enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training solutions to support the… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director, Global Marketing, Hemophilia A (ALTUVIIIO & ELOCTATE) **Location:** Cambridge, MA **About the Job** Associate Director, Global ... on ex-US markets. Serve as key business partner for initiatives with corporate affairs . + Lead congress promotional activities for ALTUVIIIO + Serve as global… more
- AbbVie (Cambridge, MA)
- …one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). + Experience ... ensure an in-depth understanding of the science behind each of these opportunities. The Associate Director, Search & Evaluation will be a key member of the Specialty… more
- AbbVie (Worcester, MA)
- …product development, Quality Systems, Product QA, Quality Control, Information Systems & Regulatory Affairs . Of experience required, must have at least 3 ... within the biologics industry; + using Quality policies, cGMP & other regulatory requirements; & + managing QC clinical & commercial projects by collaborating… more
- Takeda Pharmaceuticals (Lexington, MA)
- …information / clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial Brand teams) ... 2) medical and scientific slides housed in the Medical Affairs slide repository, and 3) other relevant publications in...and issues at sales meetings to assure legal and regulatory compliance. + Conduct strategic assessment (gap analysis) of… more