Senior CRA II – Global Multi-Sponsor Trials

3004 Syneos Health UK Limited

United Kingdom

À distance

GBP 45 000 - 65 000

Plein temps

Il y a 8 jours

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Résumé du poste

Syneos Health in the United Kingdom is seeking a CRA II / Senior CRA I for a multi‑sponsor role. The position involves site qualification, initiation, monitoring, and close‑out activities, onsite or remote, with focus on ICH‑GCP compliance and pharmacovigilance.

You will support data integrity and site readiness across multiple projects. The candidate should have a Bachelor’s degree or RN, solid GCP knowledge, strong communication skills, and be prepared to travel up to 75% regularly.

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.

Responsabilités

  • Performs site qualification, initiation, interim monitoring, site management and close‑out visits (onsite or remote) ensuring regulatory, ICH‑GCP and GPP protocol compliance.
  • Verifies informed consent procedures and protects subject confidentiality.
  • Assesses site processes, conducts Source Document Review and ensures accurate data entry in CRFs.
  • Performs IP inventory, reconciliation and verifies proper handling, labeling, import/export as required.
  • Prepares for Investigator Meetings and supports audit readiness and site training.

Connaissances

Bachelor’s degree
GCP knowledge
Computer skills
Excellent communication
Willing to travel

Formation

Bachelor’s degree or RN

Description du poste

Syneos Health in the United Kingdom is seeking a CRA II / Senior CRA I for a multi‑sponsor role. The position involves site qualification, initiation, monitoring, and close‑out activities, onsite or remote, with focus on ICH‑GCP compliance and pharmacovigilance.

You will support data integrity and site readiness across multiple projects. The candidate should have a Bachelor’s degree or RN, solid GCP knowledge, strong communication skills, and be prepared to travel up to 75% regularly.

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