Project Specialist-CTC
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Before you apply
SalaryNo pay range posted
LocationLoma Linda, CA, United States
Work modeon-site
Typefull-time
SeniorityMid
Experience2+ yrs
DepartmentClinical Trial Center
Company size10,000+ people
First seenOct 18, 2026 · 2w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
Minimum two years in clinical research administration, operations, CTMS/EMR build or study finance
Working knowledge of clinical research regulations (ICH-GCP, FDA, OHRP) and institutional workflows
Proficiency with CTMS and electronic medical record systems
Strong understanding of clinical research protocols and CMS billing requirements
Working knowledge of HIPAA guidelines
Able to read, write legibly, speak in English with professional quality
Use computer, printer, and software programs necessary to the position (e.g., Word, Excel, Outlook, PowerPoint)
Operate/troubleshoot basic office equipment
Relate and communicate positively, effectively, and professionally with others; work calmly and respond courteously when under pressure; collaborate and accept direction
Communicate effectively in English in person, in writing, and on the telephone
Think critically; manage multiple assignments effectively; organize and prioritize workload; work well under pressure; problem solve; recall information with accuracy; pay close attention to detail; work independently with minimal supervision
Bachelor's Degree in health-related field preferred
ACRP or Certified Clinical Research Professional (CCRP) through SOCRA preferred
Distinguish colors as necessary; hear sufficiently for general conversation in person and on telephone, and identify various sounds associated with workplace; see adequately to read computer screens and written documents
Skills
Oncore
LL-EAP/EPIC
CTMS
EMR
Word
Excel
Outlook
PowerPoint
About the role
Shared Services: Clinical Trial Center- (Full-Time, Day Shift) -
Job Summary: The Project Specialist supports the end-to-end operational readiness and execution of clinical research at Loma Linda by serving as a subject matter expert (SME) for Oncore and by creating and maintaining study records in LLEAP/EPIC. Partners closely with coordinators, investigators, and cross-functional teams to ensure studies are accurately built, activated, and maintained. Supports submissions to the Clinical Trial Center (CTC), advances research billing quality improvement initiatives, oversees subject stipend processes, assists the Study Startup and Study Finance teams and maintains the Center’s digital presence across institutional websites and pages. Performs other duties as needed.
Requirements
Education and Experience: Bachelor’s Degree in health-related field preferred. Minimum two years in clinical research administration, operations, CTMS/EMR build or study finance required.
Knowledge and Skills: Working knowledge of clinical research regulations (ICH-GCP, FDA, OHRP) and institutional workflows. Proficiency with CTMS and electronic medical record systems CMS Billing requirements and strong understanding of clinical research protocols. Requires working knowledge of HIPAA guidelines. Strong organizational and prioritizing skills. Able to read; write legibly; speak in English with professional quality; use computer, printer, and software programs necessary to the position (e.g., Word, Excel, Outlook, PowerPoint). Operate/troubleshoot basic office equipment required for the position. Relate and communicate positively, effectively, and professionally with others; work calmly and respond courteously when under pressure; collaborate and accept direction. Communicate effectively in English in person, in writing, and on the telephone; think critically; manage multiple assignments effectively; organize and prioritize workload; work well under pressure; problem solve; recall information with accuracy; pay close attention to detail; work independently with minimal supervision. Distinguish colors as necessary; hear sufficiently for general conversation in person and on the telephone, and identify and distinguish various sounds associated with the workplace; see adequately to read computer screens, and written documents necessary to the position.
Licensures and Certifications: ACRP or Certified Clinical Research Professional (CCRP) through SOCRA preferred.
About the company
Our mission is to continue the teaching and healing ministry of Jesus Christ. Our core values are compassion, excellence, humility, integrity, justice, teamwork and wholeness.