In-House Clinical Research Associate

Location: Cambridge, Massachusetts, United States
Salary: negotiable
Job Type: Permanent
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In-House Clinical Research Associate

Looking to make a difference in the lives of those with hard to treat diseases?

Reporting to the Director of Clinical Operations, in-house Clinical Research Associate will have a key role in helping the team reach clinical goals.

Responsibilities

  • Collaboration with sites and CROs
  • Assist in the planning, execution, and closeout of outsourced clinical trials
  • Collaborate with and assist clinical project managers to prepare all external and internal documentation for assigned trials to assure it's completed in accordance with GCP regulatory requirements and consistent with the study protocol.
  • Assist in the creation of and distribution of study materials and communicate the materials to KOLs, CROs and other external vendors.
  • Organize and prepare study files related to study tracking and reporting and submit them to the Trial Master File
  • Aid the project team with planning, preparation and possible on-site support of investigator's meetings
  • Support invoice and budget activities

Qualifications

  • Bachelor's degree with a life science or healthcare focus
  • A minimum of 2+ years of supporting clinical studies at a hospital, CRO or biopharma company
  • Strong interpersonal, organizational and multi-tasking skills; attention to detail
  • Working knowledge of ICH GCP regulations and clinical protocol

If you or someone you know feel this could be an opportunity you would like to explore please send me your most up to date resume at c.hesler (at sign) Realstaffing.com to discuss the role in further detail.

Sthree US is acting as an Employment Agency in relation to this vacancy.

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