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Clinical Research Associate II - Senior Clinical Research Associate - All US Locations - FSP

Parexel · Cheyenne, WY · Clinical Research Operations

Employment type

Full-time

Work setting

On-site

Location

Cheyenne, WY

Schedule

Day shift

Posted

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Job overview

The Clinical Research Associate (CRA) is an onsite role based in Cheyenne, WY, responsible for site management and monitoring of clinical trials. Compensation is not specified for this position, which supports the company's clinical research and site compliance efforts. This role exists to ensure patient safety and quality study execution by managing investigator sites, resolving protocol-related issues, and maintaining compliance with Good Clinical Practices (GCP) and sponsor standards.

What you'll do

  • Site management, site monitoring, close-out of clinical trials, investigator site relationship management, protocol issue resolution, and ensuring compliance with GCP and sponsor standards.

What we're looking for

Skills & competencies
full-time
day shift
cheyenne wy
clinical research
gcp
onsite
parexel
clinical trials
site monitoring
research associate
Work arrangement
  • Weekend coverage required

Why this role

Requires 2+ years of monitoring experience, FSP model, nationwide scope.

About the employer

Parexel is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.

Additional details

Industry sector
54
Industry
Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
Occupation code
11-9121.01
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