verifies site information.
Reviews patient facing materials and review translations, as directed.
Supports site staff with the vendor related qualification process, where
applicable.
Provides support by ensuring system access is requested/granted and revoked
for relevant site staff during pre-activation and subsequent course of the study.
Provides support to follow-up on site staff training, as appplicable.
Coordinates and supports logistics for IM attendance, as directed.
Supports maintenance of vendor trackers, as directed.
Coordinates study/site supply management during pre-activation and subsequent
course of the study.
Supports Essential Document collection, review and updating in systems, as
applicable.
Follows up and supports on missing study vendor data like ECGs, lab samples,
and e-diaries, as directed.
Supports ongoing remote review of centralized monitoring tools, as directed.
Supports Site payments processes by coordinating with various functional
departments within organization and site. Supports system updates and
reconciliations, as directed and follows-up on site invoices throughout the study
period.
Performs reconciliation tasks on assigned trials including but not limited to CRF
and query status, deviations, SAEs and safety reports, as applicable.
Verifies document collection status in CRG systems and drives action for
missing/incomplete/expired documents and open document findings, as directed.

May perform other assigned site management tasks, as directed by RCRA and as
per Task Matrix.
May perform a specific role profile for FSP opportunities according to Client
requests.
Maintains & completes administrative tasks such as expense reports and
timesheets in a timely manner.