Clinical Research Associate II – Multi‑Sponsor

IQVIA; Barcelona; Hybrid; EUR 32.000 - 42.000; Vollzeit

Benefits dieser Stelle

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Benefits package

Zusammenfassung

IQVIA Spain is seeking a Clinical Research Associate (junior CRA) to join our Sponsor dedicated team. You will gain experience across therapeutic areas while building a meaningful career within our organization.

You will perform site visits, support recruitment planning, ensure regulatory compliance, manage progress, and collaborate with study sites and client teams. Excellent language skills and travel flexibility are required.

Qualifikationen

• University degree in scientific discipline or health care.
• Experience in Pharma Industry, and/or Clinical Trials environment.
• Very good computer skills including MS Office.
• Excellent command of Spanish and English language.
• Organizational, time management and problem-solving skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Flexibility to travel.
• Driver’s license class B.

Aufgaben

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Kenntnisse

MS Office proficiency

Spanish language

English language

Organizational skills

Time management

Problem solving

Travel flexibility

Driver’s license B

Ausbildung

University degree in scientific discipline or health care

Jobbeschreibung

IQVIA Spain is seeking a Clinical Research Associate (junior CRA) to join our Sponsor dedicated team. You will gain experience across therapeutic areas while building a meaningful career within our organization.

You will perform site visits, support recruitment planning, ensure regulatory compliance, manage progress, and collaborate with study sites and client teams. Excellent language skills and travel flexibility are required.