- Merck & Co. (Boston, MA)
- …to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Boston, MA)
- …manufacturing to manage clinical development projectsAssist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead in ... Job DescriptionThe Clinical Director (Principal Scientist) has primary...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Takeda Pharmaceuticals (Boston, MA)
- …innovation-driven 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 and Delivery. At Takeda, we are transforming… more
- Sumitomo Pharma (Providence, RI)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director , Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management...is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators… 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 the successful...and resolve trial issues and contribute to CAPA processes. ** Site & Vendor Coordination** + Support site … more
- Lilly (Boston, MA)
- …subsidiary of Eli Lilly & Company within Lilly Research Labs, is a clinical -stage genetic medicines company established with a mission to solve the global health ... Boston, Massachusetts. **Responsibilities:** + Drive and oversee all aspects of clinical studies from planning to close-out, ensuring adherence to timelines,… more
- Parexel (Providence, RI)
- …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you will work...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical… more
- Merck (Boston, MA)
- …to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **Title: Process Engineer Small Molecules API Process Science ( Associate Director )** **Location: Cambridge, MA (Hybrid)** **About the role:** ... As a Process Engineer Small Molecules API Process Science ( Associate Director ), you will provide process engineering support in batch or continuous API platforms… more
- Sanofi Group (Framingham, MA)
- **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** Are ... aspects of medicinal product submissions + Liaises with device, clinical , manufacturing, commercial, and other internal business partners to enable… more
- Merck (Providence, RI)
- …deliver: + Increased productivity and speed to clinic/market + Accelerated timelines for site , filing, and launch readiness + Improved access to product and process ... Under the guidance of dCMC Regulatory Authoring Leadership, the Associate Principal Scientist, Regulatory Authoring Business Owner, will optimize regulatory… more
- Charles River Laboratories (Shrewsbury, MA)
- …direction and execution of daily operations in regulated preclinical and clinical space, including ligand binding assays (ie bioanalysis, immunogenicity, biomarker), ... as the primary scientific contact for internal and external clients and the on- site support of their programs. Responsible for the overall management of scientific… more
- CenterWell (Providence, RI)
- …a part of our caring community and help us put health first** The Medical Director , Primary Care relies on medical background and reviews health claims. The Medical ... Director , Primary Care work assignments involve moderately complex to...whether requested services, requested level of care, and/or requested site of service should be authorized. All work occurs… more
- Parexel (Providence, RI)
- …activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...Clinical Quality Management (CQM) as required. + Assists site in maintaining inspection ready ISF. + Prepares for… more
- Humana (Providence, RI)
- …a part of our caring community and help us put health first** The Medical Director relies on medical background and reviews health claims. The Medical Director ... or data requires an in-depth evaluation of variable factors. The Medical Director actively uses their medical background, experience, and judgement to make… more
- Parexel (Providence, RI)
- …action/preventive action (CAPA) development and checks, when applicable **Collaboration** + Reports to Director of Clinical Site Operations (DCSO) or ... **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned … more
- Humana (Providence, RI)
- …a part of our caring community and help us put health first** The Medical Director relies on medical background and reviews health claims. The Medical Director ... or data requires an in-depth evaluation of variable factors. The Medical Director actively uses their medical background, experience, and judgement to make… more
- Humana (Providence, RI)
- …Lead Medical Director , depending on the line of business. The Medical Director conducts Utilization Management or clinical validation of the care received by ... of our caring community and help us put health first** The Medical Director actively uses their medical background, experience, and judgement to make determinations… more
- Humana (Providence, RI)
- …of our caring community and help us put health first The Medical Director actively uses their medical background, experience, and judgement to make determinations ... whether requested services, level of care, and/or site of service should be authorized. All work occurs...is assisted by diverse resources, which may include national clinical guidelines, CMS policies and determinations, clinical … more
- Brockton Hospital (Brockton, MA)
- PURPOSE OF POSITION: The Director of Case Management is responsible for planning, directing, and managing of the activities of the Case Management Program for ... include the development and supervision of staff (RNs, LPN's,SWs and non- clinical support), evaluation and maintenance of case management skills and outcomes,… more