Description

- data entry portions of the clinical trials - document AEs/SAEs, patient report outcomes -read protocol assessments -handle queries -handles monitor visits and follows up with them -creating IVRS kits for nurses -At first this person will not be interacting with patients (the CRNs do this) but eventually this person will screen and recruit patients for the trials

Skills

data entry, queries, edc, clinical research coordinator, ivrs, epic, gcp, citi, medidata rave, sae, adverse event, Oncology, Gcp, Clinical research, Chart review, Pre-screening patients, Regulatory, Irb, Epic, Edc, Adverse event reporting

Top Skills Details

data entry,queries, edc, clinical research coordinator, ivrs, epic, gcp, citi, medidata rave, sae, adverse event,Oncology,Gcp,Clinical research,Chart review,Pre-screening patients

Additional Skills & Qualifications

-2 years of nursing experience -EDC system experience (Inform, MediData Rave, etc....