Clinical Research Associate II — Multi‑Sponsor Trials

IQVIA Inc; Madrid; On-site; EUR 30,000 - 45,000; Full time

Benefits offered by this job

Flexible work schedules

Therapeutic knowledge programs

Career growth resources

Mobile phone

Benefits package

Job summary

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team. The CRA will perform site visits, monitor data, and support site regulatory activities across therapeutic areas.

Ideal candidates have a university degree in a scientific field, pharma or trials experience, strong MS Office skills, fluent in Spanish and English, and willingness to travel.

The role offers opportunities for career growth within a multinational environment and flexible work options.

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

MS Office

Spanish

English

Communication

Education

University degree in scientific discipline or health care

Tools

Driver’s license class B

Job description

IQVIA Spain is seeking a Clinical Research Associate to join our Sponsor dedicated team. The CRA will perform site visits, monitor data, and support site regulatory activities across therapeutic areas.

Ideal candidates have a university degree in a scientific field, pharma or trials experience, strong MS Office skills, fluent in Spanish and English, and willingness to travel.

The role offers opportunities for career growth within a multinational environment and flexible work options.