Clinical Research Associate 2
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OverviewAs a Junior CRA at IQVIA Spain, you will support sponsor-directed clinical studies across therapeutic areas, gaining hands-on experience in site management and regulatory processes.
You will work with study sites and client teams to ensure high-quality trial execution and data integrity.
This role offers growth within a stable, international company and exposure to a wide range of trials.
You will contribute to advancing patient outcomes by helping manage trials efficiently and compliantly.
Compensaciones / Beneficiosmobile phone
career growth resources
flexible work schedules
competitive benefits package
ResponsabilidadesPerform site selection, initiation, monitoring, and close-out visits
Support development of a subject recruitment plan
Evaluate site practices for quality and regulatory compliance (GCP/ICH)
Manage progress by tracking submissions, recruitment, CRF completion, and data query resolutions
Collaborate with study-site experts and client representatives
Requisitos principalesUniversity degree in scientific discipline or health care
Experience in Pharma Industry, and/or Clinical Trials environment
MS Office proficiency
Excellent command of Spanish and English
Strong organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships
Flexibility to travel
Driver's license class B
Communication
Teamwork
Adaptability
Problem-solving
Relationship management
MS Office
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