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MONITOR CLINICAL TRIALS

Responsabilities:
Acts as primary local company contact for assigned sites for specific trials.

May participate in site feasibility and/or pre-trial site assessment visits

Attends/participates in investigator meetings as needed.

Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring),



site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies. Responsible for the implementation of analytical risk based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.

Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases. Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timeframe.

Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.

Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trial conduct.

Ensures that clinical d

📌 Monitor Clinical Trials (Ciudad de México)
🏢 Johnson & Johnson Family of Companies
📍 Ciudad de México