Monitor and own the progress of clinical studies at investigative sites
Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and
Coordinate all necessary activities required to set up and monitor a study (i.e., identify
Handle appropriately sized clinical trials, and support clinical study teams with trials that are
Train and mentor junior staff members
Interact directly with clients, initiate payments, and participate in proposal activities

🎯 Requirements

4-year college degree or equivalent experience
Holder of CRA certificate
Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical
Experience monitoring clinical trials across a variety of therapeutic areas
Availability for domestic travel including overnight stays, which may constitute up to
Fluency in English and the local language

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Healthcare Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot