The Clinical Research Associate Line Manager oversees study start-up and trial monitoring staff, facilitates hiring, training, and performance assessment, and ensures adherence to clinical trial protocols. Responsibilities include managing project timelines, quality reviews, and mentoring junior staff, while maintaining compliance with ICH/GCP guidelines.

The Clinical Research Associate executes clinical monitoring activities for oncology/hematology trials, ensuring compliance with ICH guidelines and overseeing site performance. Responsibilities include training, monitoring, and reporting, alongside collaboration with operational managers for study milestones.