We are seeking a motivated CRA to join a dynamic clinical research team. You will play a pivotal role in supporting sites and the clinical project team, acting as the main point of contact for site liaison and ensuring integrity, compliance, and excellence throughout the trial lifecycle.
Key Responsibilities
* Oversee and monitor clinical trials across multiple sites, therapeutic areas, and phases
* Develop and maintain effective working relationships with investigators, site staff, and internal project teams
* Ensure adherence to clinical trial protocols, regulatory requirements, and industry standards such as GCP and ICH
* Support submissions to ethics committees and regulatory authorities
* Maintain accurate and up-to-date study documentation and perform source data verification (SDV)
* Conduct site selection, initiation, routine monitoring, and close-out activities
* Provide study-specific training and guidance to site teams
* Monitor recruitment progress and ensure compliance with study protocols
* Prepare monitoring visit reports, follow-up communications, and other required documentation
* Identify and escalate protocol deviations or serious non-compliance issues promptly
* Collaborate with cross-functional project teams to ensure high-quality trial conduct
* Participate in process improvement initiatives, SOP reviews, and team development activities
You Will Bring
* 2–3+ years of experience as a CRA monitoring multi-centre clinical trials; experience in oncology or early-phase studies is advantageous
* Exposure to Phase I–IV trials across different therapeutic areas
* Degree in life sciences or a related field
* Strong knowledge of ICH-GCP and other relevant regulatory standards
* Excellent organizational, communication, and problem-solving skills