Irb Regulatory Coordinator Jobs in Massachusetts | ComplianceCrossing.com
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Irb Regulatory Coordinator Jobs in Massachusetts






Job info
 
Company
Lahey Clinic
Location
Burlington, MA
Posted Date
Feb 21,2018
Info Source

Coordinates multiple research studies by implementing study protocols in accordance regulatory and ... to the IRB in a timely manner. * Attends Investigator's Meetings. Reviews study content for .....

 
Company
Boston Scientific
Location
Marlborough, MA
Posted Date
Feb 18,2018
Info Source

Under direct supervision, the Clinical Trial Coordinator supports the clinical trial project team ... IRB/EC submissions, approvals and renewals. * Prepare and distribute site Regulatory binders..

 
Company
University of Massachusetts Medical School
Location
Worcester, MA
Posted Date
Feb 17,2018
Info Source

... IRB), and sponsors to ensure good clinical practice standards (GCP) throughout the life cycle of ... Manage research nurse coordinators, clinical research coordinators, and other related staff .....

 
Company
Tufts Medical Center
Location
Boston, MA
Posted Date
Feb 17,2018
Info Source

Maintains regulatory binders, case report forms, source documents, and other study documents ... Responsible for assisting with Institutional Review Board (IRB) requirements for each study .....

 
Company
Boston Medical Center
Location
Boston, MA
Posted Date
Feb 16,2018
Info Source

The Research Assistant (RA) coordinates and helps conduct device and drug treatment research trials ... all BMC IRB's policies, state and federal regulations that govern clinical research. Essential .....

 
Company
Lahey Clinic
Location
Burlington, MA
Posted Date
Feb 16,2018
Info Source

Coordinates multiple research studies by implementing study protocols in accordance regulatory and ... the IRB in a timely manner. Submits all protocol amendments / consent form revisions, adverse .....

 
Company
BAIM Institute for Clinical Research
Location
Boston, MA
Posted Date
Feb 15,2018
Info Source

... regulatory requirements, performing remote and/or on-site monitoring activities as assigned ... Coordinate and distribute amendments to sites and central IRB * Site compliance reporting of .....

 
Company
Dana-Farber Cancer Institute
Location
Boston, MA
Posted Date
Feb 15,2018
Info Source

Maintains regulatory binders and ensures study compliance with all state, federal, and IRB ... Coordination and management of clinical trials, including communication with Sponsors and .....

 
Company
Dana-Farber Cancer Institute
Location
Boston, MA
Posted Date
Feb 13,2018
Info Source

The Regulatory Coordinator (RC) works under the direction of the Principal Investigator(s ... Study Sponsor, FDA, IRB etc. Key Stakeholder Interfacing * Establishing and maintaining regular .....

 
Company
Brigham and Women's Hospital
Location
Boston, MA
Posted Date
Feb 10,2018
Info Source

The Research Coordinator is responsible for coordinating human clinical research activities for a ... In conjunction with Manager completes regulatory paperwork for institutional review board (IRB .....

 
Company
BAIM Institute for Clinical Research
Location
Boston, MA
Posted Date
Feb 06,2018
Info Source

... regulatory requirements. Perform remote and/or on-site monitoring activities as assigned and ... S. and occasional travel may be required to attend site visits, investigator and coordinator .....

 
Company
Spaulding Rehabilitation
Location
Charlestown, MA
Posted Date
Feb 03,2018
Info Source

... and coordinates the day-to-day operations of BHBIMS and plays a critical role in serving as a ... regulatory requirements for human subjects research. Ensure completion of all IRB documentation .....

 
Company
Tufts University
Location
Boston, MA
Posted Date
Jan 26,2018
Info Source

... and regulations that govern research, and protecting the University's interests. This includes ... The Institutional Review Board (IRB) is a federally mandated committee that reviews all human .....

 
Company
Brigham and Women's Hospital
Location
Boston, MA
Posted Date
Jan 21,2018
Info Source

Responsibilities include supporting CICU investigators in all of the stages of clinical research: including research initiation, regulatory (IRB) submission, care coordination of subjects, required .....

 
Company
Boston Medical Center
Location
Boston, MA
Posted Date
Jan 20,2018
Info Source

... human subject regulations. Recruits subjects to participate in the study by using approved ... Liaisons with Institutional Review Board (IRB) to facilitate approval of projects, ongoing .....

 
Company
DOCS
Location
Boston, MA
Posted Date
Jan 10,2018
Info Source

Job description  Responsible and accountable for planning, coordinating, preparing and ... IRB/EC) to study conduct, analysis and reporting  Leads the execution of clinical phases of .....

 
Company
Harbor Clinical
Location
Boston, MA
Posted Date
Jan 04,2018
Info Source

Works with site staff to obtain regulatory (IRB/IEC) approval of study specific documents Perform ... coordinates all correspondence; ensures timely transmission of clinical data with the study site .....

 
Job title
Company
Tenet Healthcare
Location
Framingham, MA
Posted Date
Dec 13,2017
Info Source

... regulations and institutional review board (IRB) requirements. The job duties include coordinating and overseeing all clinical /cooperative group trial activities from study start-up to close out for .....

 
Company
Sage Therapeutics
Location
Cambridge, MA
Posted Date
Sep 07,2017
Info Source

... FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and ... Track and ensure site IND safety letter IRB notifications; and assist in the resolution of audit .....

 
Company
University of Massachusetts Medical School
Location
Worcester, MA
Posted Date
Apr 15,2017
Info Source

... IRB submissions, summary reports, ongoing project evaluations, and coordinate arrangements ... Responsible for maintaining all regulatory paperwork from study initiation, continuation, and .....

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