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Clinical Research Coordinator I – Endocrinology
Emory University. Handle or assist with administrative activities associated with conducting clinical trials .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial administrative activities, including data management, patient recruitment, and regulatory compliance. Proficient in handling clinical specimens and maintaining accurate documentation in a healthcare setting.
Highest-signal resume keywords
Clinical Trial AdministrationData Entry and ManagementPatient RecruitmentPhlebotomyRegulatory Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data ManagementCase Report FormsQuality AssuranceClinical DocumentationPhlebotomySpecimen CollectionMedical Record ReviewInterviewing SkillsQuality-of-Life QuestionnairesScheduling Procedures
Soft Skills
CommunicationFlexibilityTeam CollaborationOrganizational SkillsAttention to Detail
Certifications & Qualifications
Licensed Practical Nurse (LPN)Clinical Researcher Credentialing
Industry Keywords
Clinical TrialsInpatient Hospital SettingHuman BloodBody FluidsInfectious MaterialsResearch Project DataPatient ContactRegulatory SubmissionsStudy MeetingsEquipment and Supplies Management
About the role
Key responsibilities & impact- Handle or assist with administrative activities associated with conducting clinical trials
- Maintain research project data, complete source documents and case report forms, and perform data entry
- Assist with patient recruitment
- Attend study meetings
- Order and maintain equipment and supplies
- Review medical records and conduct screenings for study participant recruitment
- Perform interviews and quality-of-life questionnaires
- Collect study specimens according to protocol, including phlebotomy, processing, and preparation for shipping
- Coordinate services and schedule procedures
- Create and maintain case packages
- Monitor charges
- Assist with quality assurance and track regulatory submissions
- Perform related approved responsibilities as required
Requirements
What you’ll need- High School Diploma or GED and three years of administrative support experience
- Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience
- Or a licensed practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience
- Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program
- Comfortable working in an inpatient hospital setting across multiple locations (EUH, EUHM, and Grady)
- Flexibility for occasional evening and weekend coverage
- 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
- Access to university programs and facilities without discrimination