- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring ... and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's… more
- AbbVie (Waltham, MA)
- …Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , R&D, and S&T to ensure alignment on strategic ... Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , Research and Development. Additional Information Applicable… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... for clinical deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical Program Quality… more
- AbbVie (Cambridge, MA)
- …to 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 ... one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). + Experience… 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
- 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
- Grifols Shared Services North America, Inc (Fall River, MA)
- …for the therapeutic area(s). + Partners with the Medical Directors, National MSL Sr Director , and North America Medical Affairs Sr Director to develop ... and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a...of field medical plans, strategy, and activities within Medical Affairs , as aligned with goals and objectives. This position… more
- Pfizer (Cambridge, MA)
- …design, conduct, and analysis. They work closely with other functions such as regulatory affairs , pharmacovigilance, biostatistics, and medical affairs to ... **Job Summary** The Senior Medical Director provides clinical development leadership and expertise for...the clinical development program meets the scientific, ethical, and regulatory standards. They also provides medical expertise and guidance… more
- State of Massachusetts (Boston, MA)
- …Massachusetts. The Executive Director ("ED") for the Unit reports to the Associate Deputy Commissioner of Policy & Boards ("ADC"). At the direction of the ADC, ... Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making...procedures, and policies that direct the daily licensing and regulatory activities of the boards within the Unit. The… more
- State of Massachusetts (Boston, MA)
- …misconduct. The Executive Director ("ED") for the Unit reports to the Associate Deputy Commissioner for Policy & Boards ("ADC"). At the direction of the ADC, ... Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making...procedures, and policies that direct the daily licensing and regulatory activities of the boards within the Unit. The… more