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Senior Clinical Research Associate - West Coast

Parexel · Topeka, KS · Clinical Monitoring

Employment type

Full-time

Work setting

On-site

Location

Topeka, KS

Schedule

Day shift

Posted

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Job overview

The Senior Clinical Research Associate is an onsite role based in Topeka, KS. Compensation is not specified for this position, which supports clinical trial monitoring at Parexel. This role is responsible for site management, monitoring, and close-out of clinical trials. The associate ensures patient safety and data quality by maintaining investigator relationships and ensuring compliance with GCP and sponsor standards.

What you'll do

  • Conduct site monitoring visits.
  • Ensure protocol compliance and patient safety.
  • Resolve data queries and site issues.
  • Maintain TMF documentation.

What we're looking for

Skills & competencies
full-time
day shift
topeka ks
parexel
clinical research
monitoring
oncology
gcp
travel
onsite
Work arrangement
  • Weekend coverage required

Why this role

Requires 3+ years of monitoring experience; 60-80% travel required.

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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