As a Clinical Research Associate (CRA), you will oversee and ensure the integrity of clinical research studies by monitoring data and processes, collaborating with site teams, and ensuring compliance with regulatory requirements.

Responsibilities

• Conduct site qualification, initiation, interim monitoring, site management, and close‑out visits (on‑site or remote), ensuring compliance with regulatory, ICH‑GCP, and Good Pharmacoepidemiological Practices (GPP).
• Verify informed consent procedures are properly documented and maintain confidentiality of each subject/patient.
• Perform source data verification and source document review for accurate, complete data entry in case report forms (CRFs).
• Apply remote and on‑site query resolution techniques, driving closure within agreed timelines.
• Support the use of hardware and software for effective data review and capture, and verify electronic data capture requirements.