Clinical Trial Associate Full-time Job

Creating and implementing study-specific clinical monitoring tools and documents.

Creating and overseeing the trial budget.

Identifying, enlisting, and choosing sites, and coordinating site management activities.

Coordinating and supervising clinical monitoring team.

Providing project-specific training and having regular meetings with them.

Recording and sharing interactions with clients, and acting as their representative.

Arranging and overseeing site visits.

Gathering and examining trial documents.

Assuring compliance with SOPs and local regulations, and CFR, ICH, and GCP guidelines.