CRA II: Madrid or Barcelona – Remote-Eligible

Syneos Health, Inc.

Madrid

On-site

EUR 42,000 - 56,000

Full time

9 days ago

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Job summary

Syneos Health, Inc. seeks a CRA II to support sites in Madrid or Barcelona. You will perform site qualification, initiation, monitoring, and close-out activities, ensuring regulatory and GCP compliance while maintaining data integrity and patient safety.

Travel up to 75% is required; you will collaborate with site staff and sponsor teams, prepare for audits, and contribute to trial timelines in a fast-paced, global environment. Fluency in English and Spanish is preferred for daily operations.

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Must demonstrate good computer skills and be able to embrace new technologies.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

  • Performs site qualification, initiation, interim monitoring, site management and close-out visits with regulatory and GCP compliance.
  • Verifies informed consent and safeguards patient confidentiality and data integrity.
  • Conducts source document review, data queries and ensures timely resolution with site staff.
  • Manages IP inventory, labeling and return in line with study protocol.
  • Prepares for Investigator Meetings and supports audits and training as needed.

Skills

GCP/ICH knowledge
Communication skills
Computer literacy
Travel readiness

Education

Bachelor's degree or RN

Job description

Syneos Health, Inc. seeks a CRA II to support sites in Madrid or Barcelona. You will perform site qualification, initiation, monitoring, and close-out activities, ensuring regulatory and GCP compliance while maintaining data integrity and patient safety.

Travel up to 75% is required; you will collaborate with site staff and sponsor teams, prepare for audits, and contribute to trial timelines in a fast-paced, global environment. Fluency in English and Spanish is preferred for daily operations.

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