
Laboratory: collecting, processing, coding, aliquoting and storage of blood specimens from research participants, as well as adult and pediatric phlebotomy in emergency rooms, ICU, CCU, outpatient clinics, and routine patient floors; collection, preparation and testing of throat and nasal cultures, pregnancy test, U/A and Urine cultures, as well as simple lab test: RPRs, Drug Screens, Cholesterol, A1C, CBCs, Glucose; IV insertion/HepLocks for PK studies; reagent preparation; data entry and analysis; maintenance of laboratory (sterilization of instruments, inventory, ordering supplies and equipment); maintenance of Q/A records; review of laboratory results and answering questions relating to tests and results.
Clinical Research: preparation and maintenance of regulatory documents; creating source and CRF documents, performing Q/A; transcription of CRFs (paper/database); performing clinical assessments (cognitive testing – CogFu, ADAS Cog, Mini Mental and computerized cognitive testing); evaluations and testing on research study participants (medical histories, vitals, EKGs, laboratory tests, neurological tests); lead coordinator of phase I – IV trials (beginning with the pre-site visit and ending with the closeout visit), as well as long-term storage of study documents; consenting and educating subjects on all aspects of research trials; writing recruitment scripts, FAQs, advertisements and public service announcements; documenting AEs and SAEs, as well as reporting to Investigators, Sponsors and IRB; tracking enrollment; recruitment; training individuals on take home diaries and medication usage; lead contact for internal, sponsor and FDA audits; tracking and completing queries.
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