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Clinical Research Coordinator II – Rheumatology
Emory UniversityClinical Research Coordinator managing rheumatology clinical-trial databases, participants, specimens, and regulatory submissions at Emory University. Primarily on campus in Atlanta.
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 performing phlebotomy or diagnostics as credentialed. Proficient in developing study-related documents and guiding less experienced staff in research methodologies.
Highest-signal resume keywords
Clinical Research ExperiencePhlebotomyRegulatory SubmissionsResearch Protocol ComplianceStaff Supervision
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Research Project ManagementFlow Sheet DevelopmentSource Document CompletionCase Report Form ReviewParticipant ScreeningData Collection and ProcessingStudy Specimen SupervisionRecruitment Strategy DevelopmentScheduling CoordinationAudit Accuracy
Soft Skills
Guidance and MentorshipInterpersonal CommunicationTeam Coordination
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical ResearchResearch ProtocolsParticipant ConsentRegulatory ComplianceClinical Training
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 participants according to protocol
- Approve orders for supplies and equipment maintenance
- Assist in developing recruitment strategies and 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 when appropriately credentialed and trained
- 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
- With appropriate credentialing and training, may perform phlebotomy or diagnostics
Benefits
Comp & perks- Remote work from home day options may be granted at department discretion
- Equal opportunity employment
- Reasonable accommodations for qualified individuals with disabilities