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Clinical Research Coordinator II – Infectious Diseases
Emory UniversityClinical Research Coordinator II handling administrative tasks for clinical trials at Emory University. Requires management of databases, participant coordination, and protocol compliance.
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 guiding less experienced staff. Proficient in participant recruitment, data management, and regulatory submissions.
Highest-signal resume keywords
Clinical Research ExperienceRegulatory SubmissionsPhlebotomyData ManagementParticipant Recruitment
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Case Report FormsSource DocumentsFlow SheetsSpecimen CollectionStudy Protocol Compliance
Soft Skills
GuidanceSupervisionCommunication
Certifications & Qualifications
Licensed Practical Nurse (LPN)
Industry Keywords
Clinical ResearchResearch ProtocolsEligibility DeterminationStudy ProceduresRecruitment Strategies
About the role
Key responsibilities & impact- Manages research project databases, develops flow sheets and other study related documents
- 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
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 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.
Benefits
Comp & perks- Opportunity to work from home regularly
- Flexible weekly schedule