- Dana-Farber Cancer Institute (Brookline, MA)
- …the Senior Director , Quality Assurance and Regulatory Compliance , the Director , Clinical Regulatory Compliance is responsible for the program ... program to ensure adherence to all accreditation, licensing, and clinical regulatory standards. The Director ...+ Strong knowledge of quality measurements, health care policy, clinical regulatory compliance , and patient… more
- Sanofi Group (Cambridge, MA)
- **Job Title** : Senior Director , Global Regulatory Advertising and Promotion Therapeutic Area Head **Location:** Bridgewater, NJ / Cambridge, MA (must adhere to ... progress. In this role, you will be responsible for the oversight of regulatory review of advertising, promotion, medical, media relations and other internal and… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …domestic affiliate network, (c) strategies for regional/domestic clinical growth (d) clinical joint ventures. The Associate Director will be responsible for ... closely with clinical and administrative leaders and staff. The Associate Director and their team will conduct analyses and provide expertise to inform internal… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of Nursing. This leader is accountable for APRN practice standards, regulatory compliance , credentialing, and professional advancement. He/she is accountable ... The Dana Farber Cancer Institute (DFCI) the Director of Advanced Practice Nursing provides clinical...just culture in the care environment. + Assures APRN compliance with regulatory requirements, ie licensure, credentialing,… more
- Takeda Pharmaceuticals (Boston, MA)
- …functions and external collaborators. + Lead the planning, tracking, compilation, and regulatory compliance of nonclinical technical and regulatory ... regulatory writing activities. + Represent NRWS on cross-functional teams ( Clinical , Global Patient Safety, Program Management, Global Regulatory Affairs… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulations to ensure CMC compliance within the organization + Leads regulatory compliance assessments with respect to filing requirements for assigned ... **Job Description** **OBJECTIVE / PURPOSE** + Providesprogram leadership and develops CMC regulatory strategy in support of global vaccine programs in various stages… more
- Novo Nordisk (Lexington, MA)
- …clinical experts, and Principal Investigators. Relationships Reports to: Senior Medical Director , GNAT Early Clinical Development. Work with the Early ... US Clinical Development Group, whose functions include Drug Safety, Regulatory Affairs, Clinical Operations, Medical Writing, Biostatistics, Data Management… more
- Sanofi Group (Cambridge, MA)
- **Job Title** : Clinical Research Director **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The race is on to speed ... Your skills could be critical in helping our teams accelerate progress. The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. At ... (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in...external partners. + Maintains a high standard for good clinical practice, compliance , and ethics. + Mentors… more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Quantitative Clinical Pharmacology Lead in Cambridge, MA, where you ... (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in...external partners. + Maintains a high standard for good clinical practice, compliance , and ethics. + Mentors… more
- Sanofi Group (Cambridge, MA)
- …the limits of what you thought was possible. Ready to get started? The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is ... with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery,… more
- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as the Director , Global Clinical Supply Chain Planning based in Cambridge or Lexington, MA ... new capabilities and improve existing processes/systems **_A_** **_CCOUNTABILITIES:_** + The Director (Team Lead), Global Clinical Supply Chain Planning will… more
- Bristol Myers Squibb (Cambridge, MA)
- …oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations) + Fulfills GCP and compliance obligations for ... board meetings as Early Clinical Development Physician; serves as Primary Clinical Representative in Regulatory interactions for early development projects +… more
- Brockton Hospital (Brockton, MA)
- …resources to make a difference in the lives and health of our patients. The Assistant Director , Corporate Compliance (Assistant Director ) is a member of the ... for assisting the Chief Compliance Officer (CCO) with the institutional compliance program planning and execution. The Assistant Director will utilize prior… more
- Prime Therapeutics (Boston, MA)
- …fuels our passion and drives every decision we make. **Job Posting Title** Senior Director Clinical Account Management - Remote **Job Description** The Sr ... Director of Clinical Account Management is responsible...within an organization. + Able to balance and prioritize compliance , business and other competing goals and risks, while… more
- Charles River Laboratories (Wilmington, MA)
- …build a career that you can feel passionate about. **Job Summary** The Executive Director , Corporate Compliance & Ethics role is a strategic leadership position ... and corporate functions, this role oversees the Company's global Legal Compliance (I-Comply) program, including all corporate (non- regulatory ) compliance… more
- Sunrise Senior Living (Burlington, MA)
- …clinical capability of care team members. Quality Assurance and Regulatory Compliance : + Tracks, trends, and reports clinical quality data to identify ... community. Responsible for oversight and implementation of all Care programs, regulatory compliance , recruiting, and performance management. **RESPONSIBILITIES &… more
- Novo Nordisk (Lexington, MA)
- …Operations, Non- Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external ... and manuscripts + Provide leadership in the execution of clinical trials + Ensure compliance with SOPs,...with SOPs, ICH, GCP and other national and international regulatory requirements + Work with, Clinical Operations,… more
- Dana-Farber Cancer Institute (Boston, MA)
- … clinical research and program development across the department. The Associate Director ensures compliance with all regulatory policies and guidelines ... in associated program activities, has direct supervisory responsibilities for the clinical research managers and regulatory coordinators and indirect ongoing… more
- Humana (Boston, MA)
- …and/or medical supply should be authorized. All work occurs within a context of regulatory compliance , and work is assisted by diverse resources, which may ... compliance timelines. **Required Qualifications** + 5+ years of clinical experience + Must have a current License in...10 weekends per year. **Additional Information** + The Medical Director conducts clinical reviews of the care… more