- Dana-Farber Cancer Institute (Boston, MA)
- …collection of necessary documentation and finalization of references for journal submissions . Additionally, the role involves creating visual content for grants and ... facilitating successful collaboration across various levels of an organization. + Regulatory Expertise: Strong knowledge of regulatory affairs, research ethics,… more
- WIN Waste Innovations (Brockton, MA)
- …each assigned site with administrative environmental and safety systems, reports, and submissions . What You'll Do Training and Meetings + Implement safety and ... open environmental compliance and safety issues, requests for information, regulatory interpretations, change management, etc. + Participate in school programs,… more
- Sumaria Systems, Inc. (Bedford, MA)
- …You will lead junior and mid-level personnel, ensuring alignment with regulatory requirements and best practices while assisting Government Program Managers in ... efficiency, and productivity + Support the development of statutory and regulatory acquisition reports (eg, DAES, MAR) and ensure compliance with reporting… more
- DuPont (Marlborough, MA)
- …content and contribute to the execution of key non-financial disclosures including submissions to CDP, Ecovadis, and other scorecards as needed + Monitor external ... Familiarity with sustainability rating and ranking agencies. + Knowledge of regulatory requirements related to sustainability disclosures. Join our Talent Community… more
- Astellas Pharma (Cambridge, MA)
- …understanding of pharmaceutical industry regulations and processes (eg IND, NDA submissions ). + Understanding of program management tools (eg, Microsoft Project, ... some overseas/domestic business travels. **Preferred** + Experience of interacting with regulatory authorities or preparing IND, IMPD, NDA, etc. + Proficiency with… more
- Bayer (Cambridge, MA)
- …with input from and consensus with groups such as Research, Early Development, Regulatory Affairs, and commercial functions; + Serve as an internal expert in Target ... study reports, statistical analysis plans, and clinical sections of IND/CTA submissions ; + Actively interpret clinical and clinical pharmacology data to formulate… more
- Acxiom (Boston, MA)
- …AI/ML and GenAI projects, ensuring adherence to industry standards, regulatory requirements, Responsible AI principles, and Acxiom/IPG architectural guidelines. + ... department at ###. **We highly recommend you create an account to monitor your resume submissions . Click on the Sign In link above to create an account or sign up… more
- Acxiom (Boston, MA)
- …AI/ML and GenAI projects, ensuring adherence to industry standards, regulatory requirements, Responsible AI principles, and Acxiom/IPG's architectural guidelines. + ... department at ###. **We highly recommend you create an account to monitor your resume submissions . Click on the Sign In link above to create an account or sign up… more
- Rhythm Pharmaceuticals (Boston, MA)
- …with IT/Veeva system administrator(s). + Intake product complaints, triaging submissions to differentiate between patient inquiries, patient experiences, and ... document control perspective in Veeva QDocs, ensuring documents meet procedural and regulatory requirements. + Participate in validation efforts for new or updated… more
- Veterans Affairs, Veterans Health Administration (Jamaica Plain, MA)
- …of all Resident documents to ACOS/E prior to established deadlines. Late submissions can result in disruption to the Resident rotation schedule and patient ... of health care delivery systems; Regulations and standards of various regulatory and credentialing groups; and Government-wide, agency, and facility systems and… more