Coordinating as or collaborating with Project Managers to set targets for clinical monitoring and ensuring recording of trial in compliance with project goals;
Creating and implementing study-specific clinical monitoring tools and documents;
Creating and overseeing trial budget;
Identifying, enlisting and choosing sites, and coordinating site management activities;
Coordinating and supervising clinical monitoring team;
Providing project-specific training to all trial stakeholders;
Recording and sharing interactions with clients and acting as their representative;
Arranging and overseeing site visits;
Gathering and examining trial documents;
Assuring compliance SOPs and local regulations, and CFR, ICH and GCP guidelines.

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