Histologist
Core
Train into a Clinical Research Associate (CRA I) role to deliver clinical trial monitoring work, ensuring compliance and patient safety across clinical programmes.
Role type
Trainee Clinical Research Associate (CRA I)
Builds
Clinical trial monitoring activities and study documentation for pharmaceutical sponsors
Domain
Clinical research / Pharmaceutical trials
Required skills
Clinical trial monitoring experience, Pathology Lab experience, Knowledge of ICH-GCP guidelines, Medical data review and evaluation, Study setup and coordination, Regulatory compliance
Preferred skills
None stated
Technologies
None stated
Responsibilities
Coordinate study setup and monitoring activities, Complete accurate study status reports and maintain documentation, Run sponsor generated queries and manage study cost efficiency, Develop relationships with clinical investigators and site staff, Ensure patient safety and regulatory compliance
Seniority
Entry-level (Trainee)