Sijumon Sebastian

• Counted, measured and compounded medications following standard procedures.
• Contributed to the reduction of prescription wait times by promptly addressing refill requests and insurance authorizations.
• Stocked, labeled, and inventoried medication to keep accurate records.
• Entered and processed patients' prescriptions into internal system.

* Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.

* Assist the clinical team in the preparation,handling,distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.

* Assist with the tracking and management of Case Report Forms (CRFs),queries and clinical data flow.

* Assist CRS/iCRS, CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

* May perform assigned administrative tasks to support team members with clinical trial execution.

* Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

* Assist project managers and CRA’s with developing/printing TMF binders.

* Prepared high-quality final reports upon completion of clinical trials documenting results achieved through careful monitoring of data trends.

• Supported clinical trial execution by coordinating with cross-functional teams and ensuring regulatory compliance.