
Clinical Research Coordinator II | School of Medicine - Pediatrics
- Atlanta, GA
- Permanent
- Full-time
- 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.
- Manages all research activities in support of the Section for Adolescent Medicine.
- Prepares and submits regulatory and ethics applications, including initial applications, amendments, and annual renewals to entities such as the Emory Institutional Review Board (IRB), clinical trials registries, and the National.
- Institutes of Health Develops, manages, and executes project timelines in collaboration with investigators.
- Compiles and reviews project metrics and accomplishments through the development and maintenance of research databases and reports.
- Coordinates research study-related meetings and communications.
- Manages research-related budgets, including purchasing supplies, submitting invoices, and coordinating with departmental financial analysts.
- Develops plans for program growth, including conducting landscape analyses, literature reviews, and assisting with grant preparation and submission.
- Contributes to the development and implementation of program related communications such as conference presentations, academic articles, websites, or multimedia productions.
- May participate in direct participant recruitment including performing chart reviews, informed consent, administering surveys, and conducting interviews or focus groups.
- May participate in data analysis using quantitative and qualitative methods.
- May train and supervise other research related staff including students and clinical trainees.
- Performs related responsibilities as required.
- 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 as a 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.
- Experience in a related field such as project management or clinical research.
- Knowledge of human subjects research study design and regulations.
- Ability to manage multiple priorities while working with various stakeholders.
- Accuracy and attention to detail.
- Ability to work independently with minimal oversight.
- Excellent interpersonal, organizational, and communication skills.
- Ability to work effectively in teams.