Job Details

Performance Standards. Perform all steps involved in advertising, subject recruitment, informed consent, subject enrollment, scheduling and coordination of participant visits, study visit procedures including administration of questionnaires and other information intake, checking vital signs, specimen collection, Epic order entry, visit documentation, data entry, participant reimbursement and visit documentation. Record and report adverse events and manage other communication with study participants. Support clinical data abstraction and entry via the EMR and/or any specific research databases. Support regulatory document management and submission. Additional duties as required Required Qualifications Bachelor's Degree in relevant field, ORAssociate's AND 2 years of relevant experience, OR 3 years of relevant experience, OR Equivalent training and experience Preferred Qualifications Bachelor's degree in Public Health OR currently working toward Master's Degree in Public Health. Strong ...Clinical Research, Clinical, Research, Assistant, Public Health, Healthcare