- Sumitomo Pharma (Marlborough, MA)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Parexel (Boston, MA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring… more
- IQVIA (Boston, MA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures...activities from start-up to close-out. + Escalate and resolve trial issues and contribute to CAPA processes. ** Site… more
- Parexel (Boston, MA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director, Clinical Site Startup and Engagement Process Excellence & ... Delivery based remotely reporting to the Head, Clinical Site Startup and Engagement Process Excellence...clinical research organization, with demonstrable deep understanding of clinical trial development and delivery process. +… more
- Merck (Boston, MA)
- …exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical ... Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning,...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Bristol Myers Squibb (Cambridge, MA)
- …your application should be directed to Chat with Ripley. R1597891 : Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development ... will offer the greatest possible benefit to patients. **Position Summary** The Clinical Biomarker Asset Lead role will be responsible for development and execution… more
- Sumitomo Pharma (Boston, MA)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … more
- Dana-Farber Cancer Institute (Boston, MA)
- …Research Nursing, and other departments, as needed per the requirements of the clinical trial . + Responsible for organizing and preparing for both internal ... + Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical visits, assessments, and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Research Nursing, and other departments, as needed per the requirements of the clinical trial + Responsible for organizing and preparing for both internal ... and study monitoring visits + Coordination and management of clinical trials throughout the trial life cycle,...QUALIFICATIONS:** + Bachelor's Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required. +… more