Remote CRA II (Phase III) – Home-Based, 60% Travel

Peluquería Montull

Barcelona

Remote

EUR 40,000 - 65,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Annual leave
Retirement plan
EAP LifeWorks
Life assurance
Flexible benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to support home-based trials in Spain. You will design and monitor clinical trials, ensuring patient safety and data integrity, in a sponsor-dedicated model with ICON's global expertise.

The role requires a Bachelor's degree in a scientific or healthcare field, at least 2 years as a CRA, ICH-GCP knowledge, strong organization and communication skills, and willingness to travel up to 60%.

Qualifications

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • 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 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

CRA experience
ICH-GCP knowledge
Data integrity
Travel readiness
Attention to detail
Independent yet collaborative

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate II to support home-based trials in Spain. You will design and monitor clinical trials, ensuring patient safety and data integrity, in a sponsor-dedicated model with ICON's global expertise.

The role requires a Bachelor's degree in a scientific or healthcare field, at least 2 years as a CRA, ICH-GCP knowledge, strong organization and communication skills, and willingness to travel up to 60%.

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