Clinical Research Coordinator managing administrative activities and compliance for clinical trials in the School of Medicine at Emory University. Guiding staff and interfacing with research participants.
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
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
Job title
Clinical Research Coordinator II – Emergency Medicine
Clinical Research Coordinator managing the conduct of clinical trials at Emory University. Handling administrative activities and overseeing research project requirements and compliance.
Clinical Research Coordinator at MSK, focusing on data collection and integrity for cancer research projects. Collaborating with multidisciplinary teams and ensuring compliance with regulations.
Clinical Research Coordinator providing research support for grant projects at the University of Pennsylvania. Coordinating studies on decision - making tools for misophonia and pediatric anxiety treatment programs.
Clinical Research Coordinator managing phases of clinical trials under supervision at Perelman School of Medicine. Overseeing study operations, data management, and participant recruitment in a hybrid role.
Senior Principal Biostatistician providing statistical expertise across therapeutic areas in clinical development. Collaborating with study teams and overseeing analysis plans for vital projects.
Clinical Research Assistant supporting clinical trials and participant engagement in obesity care at knownwell, Inc. Responsible for patient - facing activities to ensure high - quality experience.
Clinical Scientist Director supporting late - phase clinical development and overseeing clinical trials at Amgen. Collaborating with cross - functional teams to ensure regulatory compliance and data integrity.
Clinical Research Coordinator facilitates on - site and remote clinical studies. Ensuring adherence to protocols and managing study activities including recruitment and data management.
Senior Clinical Trial Manager managing global Phase 3 clinical trials for oncology at Verastem Oncology. Overseeing vendor management, budget adherence, and regulatory compliance throughout the project lifecycle.
Clinical Scientist Director supporting early phase clinical development at AMGEN. Collaborating to translate scientific strategy into actionable execution across clinical trials.