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Clinical Research Coordinator II – Infectious Diseases
Emory University. Handle administrative activities associated with the conduct of clinical trials .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trials, ensuring compliance with research protocols, and conducting participant screenings. Proficient in developing study-related documents and supervising research activities while maintaining high standards of accuracy and regulatory adherence.
Highest-signal resume keywords
Clinical Research ExperienceRegulatory SubmissionsPhlebotomyResearch Protocol ComplianceDatabase Management
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 Trial ManagementSource Document CompletionCase Report Form ReviewStudy Specimen ProcessingParticipant Eligibility DeterminationRecruitment Strategy DevelopmentFlow Sheet DevelopmentData AuditingClinical Training MonitoringPatient Contact
Soft Skills
Guidance to StaffCoordinationCommunicationSupervisionProblem Solving
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical TrialsResearch ProtocolsHuman Subjects ResearchInfectious MaterialsHealth Administration
About the role
Key responsibilities & impact- Handle administrative activities associated with the conduct of clinical trials
- 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 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 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
- Licensed practical nurse (LPN) and two years clinical research experience; or
- Bachelor's degree in a scientific, health related, or business administration related program and one year clinical research experience; or
- 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
- Position involves clinical patient contact and working with human blood, body fluids, tissues, or other potentially infectious materials
Benefits
Comp & perks- Equal opportunity employment
- Reasonable accommodations for qualified individuals with disabilities
- Remote work from home day options may be granted at department discretion