Cra En España

Syneos Health

Spain
Fully remote
Ich-gcp compliance
Protocol compliance
Site qualification and initiation
Syneos Health is seeking a Clinical Research Associate (CRA) for a fully remote position in Spain. The role involves overseeing clinical trial sites, ensuring compliance with regulatory standards, and supporting patient recruitment and retention strategies

Job Summary

  • Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
  • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

Matching Summary

Match Score: 85

Syneos Health is seeking a Clinical Research Associate (CRA) for a fully remote position in Spain. The role involves overseeing clinical trial sites, ensuring compliance with regulatory standards, and supporting patient recruitment and retention strategies.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • protocol compliance
  • site qualification and initiation
  • source document review
  • investigational product management
  • subject safety assessment
  • fluent in Spanish and English

Nice-to-have

  • drug development mindset
  • agile and driven to deliver
  • inclusive culture
  • passion for problem solving

Key Requirements

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
  • Knowledge of Good Clinical Practice/ICH Guidelines
  • Previous monitoring experience
  • Ability to manage required travel of up to 75%

Work Rights

Not specified

Tailored Resume

Cover Letter