CRA II – Multi-Sponsor Trials | Flexible Schedule

IQVIA Inc; Cataluña; On-site; EUR 36,000 - 48,000; Full time

Benefits offered by this job

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Benefits package

Job summary

IQVIA Spain is seeking a talented and motivated Clinical Research Associate to join our Sponsor dedicated team. You will have the opportunity to gain experience in a wide variety of therapeutic areas and build a meaningful, strong career within our organization.

Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting the development of a subject recruitment plan, evaluating regulatory compliance with GCP/ICH, and managing progress by

Qualifications

• University degree in science or health care.
• Experience in Pharma or Clinical Trials environment.
• Excellent command of Spanish and English.
• Strong organizational and time-management skills.
• Ability to travel and work with clients.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate site practices for regulatory compliance (GCP/ICH).
• Manage progress by tracking regulatory submissions, recruitment, CRF completion and data queries.
• Collaborate with study sites and client representatives.

Skills

Spanish language

English language

Site visits

Education

University degree in science/health care

Tools

MS Office

Job description

IQVIA Spain is seeking a talented and motivated Clinical Research Associate to join our Sponsor dedicated team. You will have the opportunity to gain experience in a wide variety of therapeutic areas and build a meaningful, strong career within our organization.

Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting the development of a subject recruitment plan, evaluating regulatory compliance with GCP/ICH, and managing progress by