Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms
Provides guidance to less experienced staff
Interfaces with research participants, determines eligibility and consents study participants according to protocol
Approves orders for supplies and equipment maintenance
Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires
Supervises collection of study specimens and processing
Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed
Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors
Prepares regulatory submissions
With appropriate credentialing and training may perform phlebotomy or diagnostics.
Performs related approved responsibilities as required.
Requirements
High School Diploma or GED and five years of clinical research experience
Two years of college in a scientific, health related, or business administration program and three years clinical research experience
Licensed as a practical nurse (LPN) and two years clinical research experience
Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
Master's degree, MD or PhD in a scientific, health related or business administration program.
Benefits
Premium pay eligible per departmental guidelines
On-call work required
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.