Clinical Research Associate – III

About the role

Boston Scientific is seeking a Clinical Research Associate – III to provide clinical support for the Global Clinical Operations site management team. The role works under limited supervision, ensuring that clinical trial protocols are executed in line with SOPs, ISO, GCP and other regulatory requirements. You will act as the primary liaison between the Study Core Team and the monitoring team, facilitating communication and issue resolution.

Key responsibilities

• Serve as the Site Management representative on the Study Core Team and coordinate with the monitoring team.
• Provide training and ongoing support to the monitoring team throughout the study lifecycle.
• Manage communications, monitor site‑level risks, action items and escalations.
• Schedule and conduct remote qualification, initiation, monitoring and close‑out visits.
• Perform source verification by comparing Case Report Form data with source documents and verifying informed consent forms.
• Investigate and resolve data discrepancies and ensure study compliance.
• Prepare monitoring reports, follow‑up letters, study memos and other correspondence.
• Support internal and external audits and ensure alignment of monitoring activities with study timelines and priorities.

Required profile

• Ability to work under limited supervision with general instructions.
• Strong written communication skills for clear interaction with clinical sites and project teams.
• Experience in clinical trial start‑up, enrollment, follow‑up and closure activities.

Required skills

• Knowledge of ISO and Good Clinical Practice (GCP) regulations.
• Proficiency in source verification and documentation review.