Clinical Trials Assistant

Morocco, Center, Casablanca

Reporting to the Clinical Operations Manager, your main responsibilities are to: 

• Support local study teams by providing study reports and trackers (e.g. regulatory/ethics approvals), as required.

• Working with the CSMs/CCSA, develop and maintain operational templates/tools based on the needs of assigned studies/tasks or processes

• Support document management, quality review checks and completion of country-level Trial Master File(TMF).

• Manage shared study areas (e.g. TouchPoint), according to Roche standards.

• Order study-related supplies, as delegated by the role supported, and as required.

• Support CSMs/CCSA by ensuring trial tracking systems and tools are updated so they comply with regulations, internal policies and ICH -GCP, when applicable

• Support CSMs/CCSA on startup activities.

• In collaboration with the CSMs/CSSs, coordinate local investigator and local study team meetings and departmental project/portfolio meetings, where required.

• Provide required local customs documentation to meet country requirements for importation/exportation, as applicable.

• Assist with the review and tracking of safety procedures to ensure they are being followed, escalated and resolved as necessary.

• Support management of the secure document exchange and SUSAR reporting process during the conduct of the study, as required.

• Support management of investigator, site and providers payments, if applicable.