Clinical Research Coordinator II managing research project databases and guiding staff at Emory University. Ensuring compliance with protocols and handling participant recruitment and data collection.
Responsibilities
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
Or two years of college in a scientific, health related, or business administration program and three years clinical research experience
Or a licensed practical nurse (LPN) and two years clinical research experience
Or a Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
Or a Master's degree, MD or PhD in a scientific, health related or business administration program
Benefits
Emory is an equal opportunity employer
Reasonable accommodations to qualified individuals with disabilities upon request
Job title
Clinical Research Coordinator II – Infectious Diseases
Manager overseeing Project Management team in Clinical Research at Sanford Health. Collaborating with Clinical Research Managers and guiding strategic research initiatives.
Research Coordinator overseeing clinical studies for musculoskeletal injuries in military health. Assisting with project planning and coordination while ensuring compliance with protocols and regulations.
Overseeing and administering clinical research studies and managing study budgets for military health research. Coordinating project planning and ensuring compliance with regulatory requirements.
Centralized Clinical Trial Manager at ICON responsible for reviewing clinical trial site visit reports and ensuring quality standards. Act as a liaison for timely resolution of issues.
Clinical Research Nurse Coordinator managing clinical research operations at Duke's Trauma, Acute & Critical Care Division. Supervising nursing care and ensuring accuracy in data management.
Clinical Research Coordinator managing clinical trials at Emory University. Overseeing research projects, providing guidance, and ensuring compliance with protocols and regulations.
Senior Clinical Trial Manager managing Phase 1 clinical research studies and collaborating with cross - functional teams in a global biopharmaceutical environment.
HR Manager for Clinical Research Units lead engagement strategies at Fortrea. Partnering closely with site leadership in clinical environments in Dallas, TX or Madison, WI.
Clinical Trial Manager overseeing clinical trials managing operations and compliance in Brazil at IQVIA. Ensuring adherence to protocols and managing country - specific requirements.