Vacancy Description
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....
- 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....
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