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Clinical Research Coordinator II – Human Genetics
Emory UniversityClinical research coordinator managing clinical trial databases, participants, specimens, and regulatory submissions at Emory University. Supporting Human Genetics research in Atlanta.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trials, including participant recruitment, regulatory submissions, and compliance with research protocols. Proficient in handling clinical research documentation and providing guidance to staff while ensuring accurate data collection and processing.
Highest-signal resume keywords
Clinical Research ExperienceRegulatory SubmissionsParticipant RecruitmentPhlebotomyCompliance Monitoring
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ManagementSource Document CompletionCase Report Form ReviewStudy Protocol ComplianceData Accuracy Auditing
Soft Skills
Guidance to StaffInterpersonal CommunicationTeam Coordination
Tools & Technologies
Research Project DatabasesFlow SheetsStudy-Related Documents
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical TrialsInformed ConsentParticipant ScreeningStudy Specimen ProcessingRegulatory Documents
About the role
Key responsibilities & impact- Handle administrative activities associated with conducting clinical trials
- Manage research project databases and develop flow sheets and study-related documents
- Complete source documents and case report forms
- Provide guidance to less experienced staff
- Interface with research participants, determine eligibility, and obtain informed consent according to protocol
- Approve orders for supplies and equipment maintenance
- Assist with recruitment strategies and conduct participant screenings, interviews, and questionnaires
- Supervise collection and processing of study specimens
- Establish case packages for study procedures
- Monitor procedure scheduling and charges and coordinate other services as needed
- Ensure compliance with research protocols
- Review case report forms and audit accuracy against source documents
- Attend sponsor monitoring meetings
- Prepare regulatory submissions
- Perform phlebotomy or diagnostics with appropriate credentialing and training
- Perform related approved responsibilities as required
Requirements
What you’ll need- 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
- Preferred: experience with recruitment, coordinating complicated clinical trials, and managing regulatory documents
- Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher
- Clinical patient contact and work with laboratory materials, including human blood, body fluids, tissues, or other potentially infectious materials
Benefits
Comp & perks- Equal opportunity employer
- Reasonable accommodations for qualified individuals with disabilities
- Potential remote work-from-home day options at department discretion