Work in Health care domain, where I can use my expertise for the potential growth of the organization and self.
• Coordinates approval of new study agreements and contracts.
• Completes case report forms. Extracts data from patient file (Source documents) in a timely manner.
• Responds to data clarification requests in a timely manner.
• Performs specimen processing and shipment of biological specimen duties.
• Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
• Reviews and comprehends each assigned protocol including study proceedings and timelines.
• Study subject appointments and serves as the patient liaison to the PI and other participating physicians.
E-crf Used
·Octalsoft · XIP · I-medideta
· RTSM · Clinidox · Dignosearch
· Connect · Endpoint · Clinion
· HOTS · Inform · Preclarus ppd
· Redcap · Nukleus
· Oracle
· Almac
• Good writing and communication skills.
• Knowledge of MS Office and Internet application.
• Medical Terminology.
• Working under deadlines & strongly adaptable.
• Willingness to learn, positive attitude in facing new challenges.
• Team player.
• ICH-GCP