Job Description: Responsibilities Job Title: Clinical Study Manager Reports to: Director of Clinical Studies... FLSA Status: Exempt Job Summary A Clinical Study Manager (CSM) is responsible for overseeing the planning, execution...
Job Description General Summary: The Clinical Study Quality Lead Senior Manager conducts quality assurance... oversight and management activities of clinical trial operations to ensure Vertex trials are conducted in accordance with Good...
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse...
, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse... and dynamic team. As a Manager of Study Start-Up at ICON, you will lead and oversee the start-up activities for clinical trials...
Manager, Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... to shape the future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse...
Manager, Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... to shape the future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse...
and daily lives. As the Project Manager, Clinical Trials, you will play a key role in supporting the execution of WHOOP...-sponsored clinical studies. You will manage day-to-day project operations, including study timelines, budgets, regulatory...
study teams and clinical subteams to meet enrollment and study delivery timelines. You will work with other functional... as needed within clinical study teams. KEY POSITION RESPONSIBILITIES Support the GDL in the execution of the clinical development strategy...
: As Manager, Clinical Trial Site Budget and Contracts, you are responsible for developing and negotiating investigator site... budgets, as well as coordinating execution of clinical trial agreements. This position serves as a liaison for budget...
profession Minimum 4 years of professional experience in pharma/biotech as a Clinical Study Manager, Project Manager, CRA.../Clinical Monitor or in a similar function, with experience coordinating a cross functional team for study execution (Phase 1-3...
Position Overview Bicara Therapeutics is seeking a Manager - Senior Manager of Clinical Supply Chain to lead clinical... in-office days each week. Key Responsibilities Develop, own, and execute end-to-end clinical supply chain strategies...
Clinical Process Excellence Manager - Contract - Cambridge, MA Do you have the vision and drive to transform clinical..., and efficiency in clinical study management. You will also contribute to training, process improvement initiatives, and governance...
Director of Clinical Data Management, the Senior Manager of Clinical Data Management will be responsible for managing clinical... data management activities across Tango's clinical trials. This includes overseeing study-specific data management...
better, longer. For more information, visit us at . About the Role Senior Manager, Clinical Supply Chain The Senior Manager..., Clinical Supply Chain will play a critical supporting role in the execution and coordination of clinical supply activities...
About the role: The Senior Manager, Clinical Strategist for real-world evidence (RWE) plays a pivotal role in shaping... expert in translating clinical need to RWE regulatory use cases, providing best practices for RWE study development...
for assisting the Clinical Research Manager with the oversight of their disease group’s clinical trial portfolio and all related...Responsibilities Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible...
authoring complex clinical study documents and sections of regulatory submissions to support all phases of clinical drug... activities. Key Duties and Responsibilities: Authors complex clinical regulatory documents (e.g., clinical study protocols...
guidance to clinical data management personnel on assigned projects, reviewing study documents as needed, e.g. Data Management...Responsibilities: Responsible for the study-specific data management tasks from protocol review to database lock...
review of the study statement of work, RFPs, budgets, and Change Orders. Works with the CRO to ensure the clinical data...Responsibilities: Responsible for the oversight of all data management CRO activities supporting company's clinical...
Responsibilities: Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out... thinking, alignment-building and discretion to tailor documents to study needs. Independently lead data cleaning activities...