NEHA RAJI JOHN

• Performed Pharmacovigilance and Materiovigilance activities with the objective of improving patient safety.
• Prepared chemotherapeutic drug mixing in accordance to individual patient regimens.
• Formulated and implemented Standard Operating Procedures (SOP) during poison protocols.
• Dispensed powdered form of tablets to neonates, infants and children through the process of dose division.
• Received, handled and resolved inter-departmental references, drug information queries and drug dosage computations.

• Conducted patient recruitments and subsequent visits in accordance with GCP guidelines and the proposed protocol.

• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Gathered, processed, and shipped lab specimens.
• • Communicated and coordinated effectively with the Clinical Research Associate, Principal Investigator, Substitute- Investigator and other healthcare professionals to support clinical trial data accuracy..

• Conducted a final review and managed all the close-out procedures.