Study coordinator jobs in Boston, MA

Apply Job Type Full time Description Under the direction of The Fenway Institute's Associate Medical Director and the Clinical Research Operations Manager, the Study Coordinator will work with..

Position. Research Study Coordinator, Infectious Diseases Location. Boston, MA Schedule. 40 hours per.. POSITION SUMMARY. The Study Coordinator is responsible for on. and off site study implementation and..

The TIMI Research Coordinator is responsible for coordinating human clinical research activities, for.. submit all study documentation in a timely manner to appropriate data management and core laboratories..

The TIMI Research Coordinator is responsible for coordinating human clinical research activities, for.. submit all study documentation in a timely manner to appropriate data management and core laboratories..

The Study Coordinator will work with the research team under the direction of the Principal Investigator.. Responsibilities. Monitor and track study activities to be shared with principal investigators and study..

STUDY COORDINATOR, School of Medicine, Neurology Tracking Code Job Description The BU CTE Center seeks a.. manage regulatory documents, communication with IRB and study sponsors, screen, and recruit study..

Provide client insights on pre clinical testing regulations. Act as an autonomous Study Director.. Interpret local regulations and expand service offerings accordingly. Supervise study processes from..

Financial Outcome. Develops and monitors study budget and timelines. Manages budgetary spend of the.. Monitors study progress, ensuring compliance with and adherence to the project plan, while identifying..

Overview The Eliot Pearson Department of Child Study and Human Development is committed to strengths.. What You'll Do Under minimal supervision, the Program Coordinator provides advanced administrative..

Clinical Research Coordinator BWH TIMI Study (3286288)DescriptionThe TIMI Research Coordinator is.. submit all study documentation in a timely manner to appropriate data management and core laboratories..

Provide client insights on pre clinical testing regulations. Act as an autonomous Study Director.. Interpret local regulations and expand service offerings accordingly. Supervise study processes from..

Will provide direct care to patients enrolled in studies. Will utilize nursing and study knowledge to.. Complete and maintain study documentation. PRINCIPAL DUTIES AND RESPONSIBILITIES The research nurse..

Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.Come join a fantastic Team! The Clinical Study Manager is..

Come join a global leader in drug development!. We have a great opportunity for a STUDY DIRECTOR I.. Be a part of this life saving work.Some of the duties include Serves as a Study Director for a wide..

Full time, TemporarySTART DATE. Friday, April 26, 2024 (flexible start day)END DATE. Monday, May 6, 2024ObjectiveModerators are expected to interact directly with study participants using..

Candidates will interact with a new AI chatbot during the research study. The task is estimated to take six hours in total, the first hour is for the introduction and delivery of instructions..

Title. Associate Clinical Study Manager Type. Contract to Hire Duration. 6 months. (could convert to.. Job Summary. Clinical Study Associate Manager supports the study team by taking responsibility for areas..

Hobson Prior are currently looking for a Senior Clinical Study Manager to join a brilliant biotech.. For this role, you will be accountable for the selection and management of CROs and study connected..