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An Associate, Site Manager is an entry level site management role with typically 2 years of

experience in site monitoring. This role serves as the primary contact point between the Sponsor and the

Investigational Site. An Associate, Site Manager is assigned to trial sites to ensure inspection

readiness through compliance with the clinical trial protocol, company Standard Operating

Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines

from study start-up through to site closure. Responsibilities may include assisting with site

selection, site qualification assessment, subject recruitment and retention planning, site

initiation, on-site and remote monitoring and close-out activities. The Associate, Site Manager

will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial

Delivery Leader) to ensure overall site management while performing trial related activities for

assigned protocols. May contribute to process improvement and training. Some supervision

from a more Senior, Site Manager (Senior SM or Lead SM) to help provide guidance to

Associate, Site Manager.