FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
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 screenings and interviews. Proficient in developing study-related documents and coordinating services while providing guidance to less experienced staff.
Highest-signal resume keywords
Clinical Research ExperienceParticipant ScreeningRegulatory SubmissionsPhlebotomyCompliance Monitoring
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 ReviewSpecimen ProcessingParticipant Eligibility DeterminationRecruitment Strategy DevelopmentClinical Training MonitoringDiagnostics PerformanceClinical Patient Contact
Soft Skills
Guidance to StaffInterpersonal CommunicationCoordination Skills
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical ResearchHuman Blood HandlingInfectious MaterialsResearch Protocol ComplianceStudy Procedures
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 participant 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 monitoring meetings with sponsors
- 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 as a 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
- Position involves clinical patient contact
- Experience working with human blood, body fluids, tissues, or other potentially infectious materials
Benefits
Comp & perks- Equal opportunity employer
- Reasonable accommodations for qualified individuals with disabilities
- Participation in university programs and use of facilities without discrimination