We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!
This role is to be based inBarcelonaarea.
Key Responsibilities:
In this role you will
Monitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirements
Build strong relationships with investigators and site staff
Ensure high-quality data collection and patient safety
Work closely with the sponsor providing insights and updates on study progress
Perform on-site monitoring visits
Qualifications:
University or college degree or certification in a related allied health profession from an appropriately accredited institution (Fortrea may consider relevant and equivalent experience in lieu of educational requirements)
Minimum 2 years of experience as CRA in Spain; experience in oncology and ideally CAR - T studies.
Thorough understanding of ICH GCP Guidelines of local regulatory requirements and of monitoring procedures.
Basic understanding of the clinical trial process.
Fluent in Spanish and in English both written and verbal.
What We Offer:
Competitive salary and performance bonuses
Career growth environment in a supportive environment
Works directly with a leading sponsor on innovative studies
Ready to take your CRA career to the next level Apply now!
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!This role is to be based inBarcelonaarea.Key Responsibilities:In this role you willMonitor clinical trial sites to ensure compliance with protocols GCP and regulatory requ...
We are seeking aSponsor-Dedicated CRA IIwith solid monitoring experience. If you are eager to make an impact this is your chance!
This role is to be based inBarcelonaarea.
Key Responsibilities:
In this role you will
Monitor clinical trial sites to ensure compliance with protocols GCP and regulatory requirements
Build strong relationships with investigators and site staff
Ensure high-quality data collection and patient safety
Work closely with the sponsor providing insights and updates on study progress
Perform on-site monitoring visits
Qualifications:
University or college degree or certification in a related allied health profession from an appropriately accredited institution (Fortrea may consider relevant and equivalent experience in lieu of educational requirements)
Minimum 2 years of experience as CRA in Spain; experience in oncology and ideally CAR - T studies.
Thorough understanding of ICH GCP Guidelines of local regulatory requirements and of monitoring procedures.
Basic understanding of the clinical trial process.
Fluent in Spanish and in English both written and verbal.
What We Offer:
Competitive salary and performance bonuses
Career growth environment in a supportive environment
Works directly with a leading sponsor on innovative studies
Ready to take your CRA career to the next level Apply now!
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
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