- General Motors (Providence, RI)
- …three times a week, at minimum. **The Role:** The Employee Relations Investigator will perform investigations of misconduct, and/or violations of policy. The ... Investigator will work closely with the HR Policy and...5 years of professional experience in Human Resources, or Corporate Global Investigations + Perform investigations of alleged misconduct… more
- Takeda Pharmaceuticals (Boston, MA)
- …quality control reviewers, and functional service providers (FSPs) to meet corporate goals and successfully execute on high-quality deliverables across all programs ... cycle times. + Apply advanced knowledge of relevant regulatory requirements and corporate policies, as well as work experience, to assess document requirements and… more
- Merck (Providence, RI)
- …(ED) for Field Medical Affairs in the US understands our Company's corporate and products/portfolio strategies and work cross-functionally with the Global Medical ... and increase participation in studies of Our Company compounds by increasing investigator awareness of research opportunities supported by Our Company + Support Our… more
- Actalent (Boston, MA)
- …for direct client/customer management including business retention and maintenance * Lead clinical operations activities for assigned employees and or programs ... ensuring compliance with GCP, ICH and applicable regulations; may lead the development of all study related plans necessary for trial conduct * Develop project… more
- Sumitomo Pharma (Providence, RI)
- …launch activities related to Medical Affairs function. This individual will lead program coordination with Clinical Development leadership to ensure alignment ... motivation, and control of activities in alignment with the company's corporate strategies and objectives. + Ensure cross-functional medical alignment with the… more
- Rhythm Pharmaceuticals (Boston, MA)
- …Head of Medical Writing. Responsibilities and Duties + Author and serve as lead writer for complex clinical and regulatory documents (eg, protocols and amendments, ... clinical study reports, Investigator 's Brochures, regulatory submissions and responses to health authority...complex global programs + Serve as the Medical Writing Lead on cross-functional core program teams + Ensure accuracy… more
- Sumitomo Pharma (Providence, RI)
- …internal company programs and external facing interactions. This job will effectively lead and communicate with cross-functional team members to develop and execute ... communication, education and awareness stakeholders. + Serve as a Medical Strategy lead for the Pfizer alliance for Prostate, ensuring coordination and alignment of… more
- Rhythm Pharmaceuticals (Boston, MA)
- …ensuring compliance, and quality execution of clinical trials. The individual will lead and/or support GCP audits, maintain inspection readiness, and manage key ... during the various audits + Independently conduct audits, including Clinical Investigator Site Audits, GCP Document Audits, and support Internal Process Audits… more