Remote Clinical Research Associate II - Spain | 60% Travel

Institute for Bioengineering of Catalonia (IBEC)

Barcelona

Remote

EUR 42,000 - 56,000

Full time

2 days ago
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Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II for a home-based role in Spain. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and data integrity while safeguarding patient safety.

Collaborate with investigators and staff to ensure smooth study conduct, review data and resolve queries, and contribute to study documentation.

Qualifications

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required (approximately 60%).

Responsibilities

  • Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high‑quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

ICH-GCP knowledge
Data integrity
Travel readiness
Independent and team player
Strong communication
Organizational skills

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II for a home-based role in Spain. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and data integrity while safeguarding patient safety.

Collaborate with investigators and staff to ensure smooth study conduct, review data and resolve queries, and contribute to study documentation.

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