Senior CRA II – Multi-Sponsor Clinical Trials

IQVIA; Madrid; On-site; EUR 38,000 - 54,000; Full time

Benefits offered by this job

Mobile phone

Benefits package

Job summary

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team in Madrid. The successful candidate will conduct site selection, initiation, monitoring, and close-out visits, while supporting recruitment plans and ensuring regulatory compliance across multiple therapeutic areas.

Ideal candidates have pharma/clinical trials experience, strong MS Office skills, and fluency in Spanish and English. Travel flexibility and a valid B-class driver’s license are required.

Qualifications

• 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

Responsibilities

• 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

Skills

Spanish fluency

English fluency

Site monitoring

Regulatory knowledge

Education

University degree in scientific discipline or health care

Tools

MS Office

Job description

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team in Madrid. The successful candidate will conduct site selection, initiation, monitoring, and close-out visits, while supporting recruitment plans and ensuring regulatory compliance across multiple therapeutic areas.

Ideal candidates have pharma/clinical trials experience, strong MS Office skills, and fluency in Spanish and English. Travel flexibility and a valid B-class driver’s license are required.