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Clinical Research Coordinator II – Endocrinology
Emory University. Manage research project databases .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research projects, ensuring compliance with protocols, and conducting participant interactions. Proficient in data management, regulatory submissions, and clinical training oversight.
Highest-signal resume keywords
Clinical Research ExperienceRegulatory SubmissionsPhlebotomyData ManagementParticipant Screening
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchData ManagementPhlebotomySource Document CompletionCase Report Form ReviewStudy Protocol ComplianceParticipant Eligibility DeterminationRecruitment Strategy DevelopmentSpecimen CollectionClinical Training Monitoring
Soft Skills
Guidance to StaffInterpersonal CommunicationFlexibilitySupervisionCoordination
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical ResearchInpatient Hospital SettingHuman BloodBody FluidsTissuesInfectious MaterialsStudy ProceduresSponsor MonitoringCase PackagesStudy Specimens
About the role
Key responsibilities & impact- Manage research project databases
- Develop flow sheets and other study-related documents
- Complete source documents and case report forms
- Provide guidance to less experienced staff
- Interface with research participants
- Determine eligibility and consent study participants according to protocol
- Approve orders for supplies and equipment maintenance
- Assist in developing recruitment strategies
- Conduct participant screenings, interviews, and questionnaires
- Supervise collection and processing of study specimens
- Establish case packages for study procedures
- Monitor scheduling of procedures and charges
- 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
- Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher
- Comfortable working in an inpatient hospital setting across multiple locations (EUH, EUHM, and Grady)
- Flexibility for occasional evening and weekend coverage
- Position involves clinical patient contact and working with human blood, body fluids, tissues, or other potentially infectious materials
Benefits
Comp & perks- Equal opportunity employment protections
- Reasonable accommodations for qualified individuals with disabilities
- Access to university programs and facilities without discrimination