Senior CRA I – Global Trials & Mentorship

IQVIA Inc

Barcelona

On-site

EUR 28,000 - 38,000

Full time

4 days ago

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Job summary

IQVIA is seeking a Senior Clinical Research Assistant I to join our CFSP team in Barcelona. This role involves on-site monitoring across trials, ensuring data integrity and patient safety while building strong investigator relationships.

A life sciences degree with 3–5 years of on-site CRO experience is required, along with GCP/ICH knowledge and travel up to 40–60%. You will mentor junior staff, support study start-up and close-out, and collaborate with cross-functional teams to meet project

Qualifications

Bachelor's or higher in Life Sciences, Health Sciences, Nursing, Pharmacy, or related field.
3–5 years on-site monitoring experience in CRO/pharma/healthcare.
Strong knowledge of GCP and ICH guidelines.
Experience in sponsor-dedicated or cfSP environments preferred.
Knowledge of patient recruitment and start-up activities preferred.

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits per protocol and GCP/ICH guidelines.
Ensure patient safety, data integrity, and study quality at sites.
Build relationships with investigators and site staff; provide training and support.
Monitor progress, regulatory docs, recruitment, data queries, and site metrics.
Collaborate with sites to optimize recruitment and timelines.
Maintain inspection-ready study docs (ISF, TMF, monitoring reports).
Escalate risks and issues; drive timely resolutions.
Work with cross-functional teams to support study delivery.
Mentor junior staff through coaching and co-monitoring.
Support start-up, maintenance, close-out, and site financial activities.