Conducts monitoring (pre-study, initiation, routine monitoring and closeout visit), if require

Conducts co-monitoring visits, if required

Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.)

Completes monitoring visit reports timely

Assists with investigator/site identification

Assists site to prepare Institutional Review Board/Ethics Committee (IRB/EC) submissions

Facilitates clinical trial site contract and budget negotiation

Accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability

Manages site queries and communications

Provides protocol and related study training...