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Clinical Research Monitor

System One
Boston, MA
  • Posted: over a month ago
  • Contractor
Job Description

Title: Clinical Research Monitor

Location: Boston, MA (TIMI Study Group) *Remote Role*

Start date: ASAP

Responsibilities: Contract to Hire



BS Degree in Science or Healthcare related field required


Minimum of 5 yrs. clinical trial related exp. for large, multi-center national and/or international clinical trials.

Ideally exp. with Cardiovascular studies and/or medical terminology preferred


Previous Clinical Monitoring experience

Knowledge/exp. with Electronic Data Capture Systems (i.e. inform, IWRS, eCOS or similar)

Willingness and ability to travel to trial sites as required
Must have worked in a Cardio clinical trial

Working knowledge of HIPAA

“Nice to Haves”:

- Certified Clinical Research Professional(CCRP) or equivalent and/or Certified Clinical Research Associate(CCRA) preferred but not required
- Experience with cardiovascular studies and medical terminology preferred

Primary Duties/Responsibilities:

Conduct between 8-10 field visits per month. Travel is depended on study specific needs. (will be assigned a region/territory. Also sites are US Based only)

Ensure the assigned site study staff conduct the study in compliance with the currently approved protocol/amendments and trial operations manual.

Perform on-site visits, such as qualification, site initiation, interim monitoring and study close-out visits

May also include observation of participant visits, performing source document verification, query resolution, triaging site issues, conducting staff training and collaborating with in-house clinical trial protocol coordinators to ensure regulatory documents and ISF’s are complete

Perform document verification/review in accordance with the Monitoring Plan

System One


Boston, MA



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