Clinical Research Associate II

Precision Medicine Group

Clinical Research Associate II monitoring clinical studies for Precision Medicine Group based in Spain. Ensuring compliance, coordinating activities, and managing clinical trial progress with travel commitments.

Posted 7/3/2026full-timeRemote • 🇪🇸 SpainJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)

Requirements

What you’ll need

4-year college degree or equivalent experience
2 (two) years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies.
Site management or equivalent experience in clinical research
Oncology monitoring experience
Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
Fluency in English and for non-English speaking countries the local language of country where position based
Candidates must reside in Madrid or Barcelona

Benefits

Comp & perks

Flexible working hours
Professional development opportunities

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

Clinical Study MonitoringProtocol ComplianceSOP AdherenceICH-GCP KnowledgeRegulatory Requirements