Clinical Research Associate – CFSP (CRA II)

Vall d’Hebron Institute of Research (VHIR) - Vall d'Hebron Institut de Recerca

Barcelona

On-site

EUR 45,000 - 65,000

Full time

12 days ago

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Job summary

IQVIA is recruiting a Clinical Research Associate for CFSP in Madrid/Barcelona. You will monitor trials, maintain site relationships, and ensure data integrity across multiple therapeutic areas. The role requires on-site experience, strong GCP knowledge, and willingness to travel up to 40–60% with a valid driving license.

Join a global team, engage in structured training, mentorship, and clear career pathways in clinical research.

Qualifications

Bachelor-level or higher in Life Sciences, Health Sciences, Nursing or Pharmacy.
1.5 years plus on-site monitoring experience in CRO/pharma/biotech.
Solid knowledge of GCP, ICH guidelines and regulatory requirements.
Experience in a sponsor-dedicated cfSP environment is a plus.

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits per protocol and guidelines.
Ensure patient safety, data integrity, and protocol compliance.
Maintain relationships with investigators and site staff; provide training and support.
Monitor recruitment, regulatory docs, data queries, and site performance metrics.
Collaborate with sites to optimize patient recruitment and retention.
Maintain inspection-ready TMF/ISF documentation and study files.
Escalate risks and site issues; drive timely resolutions.
Partner with cross-functional teams to support study delivery.
Mentor junior team members through coaching and co-monitoring.