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Clinical Research Coordinator
GE HealthCare. Recruit, screen, enroll, and obtain informed consent from study participants .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research coordination, including participant recruitment, compliance with regulations, and management of study documentation. Proficient in maintaining databases and facilitating training while ensuring adherence to ethical standards and internal processes.
Highest-signal resume keywords
Clinical Research ExperienceParticipant RecruitmentRegulatory ComplianceMicrosoft Office ProficiencyCCRC or CCRP Certification
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 ResearchParticipant ScreeningData ManagementDocumentation MaintenanceProcess ImprovementUltrasound ScanningEthics Committee ApplicationsStudy Protocol ComplianceTraining CoordinationAudit Preparation
Soft Skills
Outstanding Organizational SkillsMeticulous Attention to DetailExcellent Communication SkillsFlexibility in Scheduling
Tools & Technologies
Microsoft ExcelMicrosoft OutlookMicrosoft Word
Certifications & Qualifications
CCRCCCRP
Industry Keywords
GCPEthics CommitteeVolunteer DatabaseResearch Program IntegratorsStudy Materials
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Recruit, screen, enroll, and obtain informed consent from study participants
- Maintain the volunteer database and manage recruitment efforts
- Coordinate and oversee research sessions, including participant scheduling, space reservation, staff training, and documentation
- Ensure compliance with study protocols, regulations, GCP, Ethics Committee requirements, and internal GEHC processes
- Maintain regulatory binders, source documentation, trackers, and other study materials
- Assist the Principal Investigator with Ethics Committee applications and submissions
- Conduct training and guide study staff
- Facilitate monitoring visits and prepare for audits
- Serve as the main point of contact for research volunteers and study staff
- Maintain consent areas and scan bays, order supplies, and track spending
- Implement process improvements and electronic compliance processes
- Support Research Program Integrators
- Serve as a subject matter expert for coordinators at global sites
- Manage in-house ultrasound scanning sessions for GEHC Ultrasound Businesses in Horten and Oslo
- Be physically present in Horten and Oslo during ultrasound scanning sessions
Requirements
What you’ll need- Bachelor's degree in social, life science, or research related fields
- Minimum of 1 year of experience in clinical research
- Outstanding organizational skills
- Proficiency in Microsoft Office (Excel, Outlook, Word)
- Meticulous attention to detail
- Excellent written and verbal communication skills
- Flexibility in scheduling
- CCRC, CCRP or equivalent certification preferred
Benefits
Comp & perks- Total rewards package including salary and benefits
- Career opportunities
- Culture that fosters care, collaboration and support
- Relocation assistance not provided