Senior Clinical Research Associate – All US Locations

Parexel

Clinical Research Associate managing clinical studies and ensuring compliance with client procedures and international regulations. Collaborating with study teams to monitor and close assigned sites effectively.

Posted 6/6/2026full-timeRemote • North Carolina • 🇺🇸 United StatesSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD)
The CRA acts as the main contact with the study site
Responsible for monitoring the study conduct
Responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies
Ensures compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations

Requirements

What you’ll need

Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
Excellent attention to detail
Good written and verbal communication skills
Proficient in written and spoken English language required
Fluency in local language(s) required.

Benefits

Comp & perks

Health insurance
Paid time off
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

monitoringstudy conductpreparationinitiationclosurecomplianceICH-GCP

Soft Skills

attention to detailwritten communicationverbal communication