Clinical Research Associate – 2

Grifols

Clinical Research Associate assisting with clinical trial monitoring and ensuring regulatory compliance. Coordinating study activities and collaborating with data management to track trial progress.

Posted 5/19/2026full-timeNC-RTP • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Assists in the management of the clinical monitoring process
Ensures coordination of study start-up
Tracking study specific tasks and progress of the trial
Performing regulatory document review and approval
Conducting monitor training

Requirements

What you’ll need

Associate’s degree in a life science field required
Bachelor’s degree in a life science field preferred
Typically requires 2 years of experience in clinical research
Minimum of 1 year field monitoring experience
Good knowledge of medical terminology, protocol, clinical trial process
Strong knowledge of ICH/GCP Guidelines and EDC process

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory document reviewmonitor trainingclinical trial processfield monitoring

Soft Skills

coordinationtrackingmanagement