Review of Protocol, Study Documents. Undertake the preparation and submission of EC dossier to ECs. Review of EC approval letter for trial to ensure the accuracy of documents version number. Identify, Screen and select potential investigator and vendors for the conduct of clinical trials. Site FeasibilitySite selection visit. Site Initiation Visit. Onsite Monitoring Visit (To perform SDV, CRF review, IP accountability, review of AE and SAE, ensure compliance with protocol, SOPs and regulatory requirements. identify the Protocol deviation) Conduct of Remote Monitoring Close Out Visit. Ensured the sites raised the invoices as per the CSA/CTA on timely basis with timely payment.Maintain audit readiness at any time point. Preparation of monitoring plan. Training of other team member on Monitoring SOPs, Guidelines, Protocols and other study documents.

Patients recruitment & Follow - up , Coordinates subjects test & procedure,Maintain study documentation (Consent form, Source documents,case report form (CRF), Drug accountability )