Clinical Research Coordinator (1142121)

Description

Position Overview
We are seeking an experienced Clinical Research Coordinator to support and manage clinical research studies focused on liquid biopsy testing for GI cancer detection. This is a patient-facing role requiring hands-on clinical research experience in a site-based research setting where study participants are seen and managed onsite. The ideal candidate will have strong clinical trial experience, excellent organizational skills, and a team-oriented attitude with the flexibility to assist wherever needed.

Must-Have Qualifications

• Minimum 2+ years of clinical research/clinical trials experience
• Experience working in a patient-facing clinical research environment
• Phlebotomy experience required
• Experience with study documentation, data collection, and regulatory compliance
• Knowledge of clinical trial protocols and FDA guidelines
• Strong interpersonal, communication, and organizational skills
• Ability to work independently while supporting a collaborative team environment

Preferred Qualifications

• Bachelor's degree required (4 years of relevant clinical research experience may be considered in lieu of a degree)
• Experience with pharmaceutical-sponsored clinical trials
• Experience using EMR systems
• Proficiency in Microsoft Office Suite
• Experience supervising or guiding Research Assistants

Key Responsibilities

• Coordinate and support clinical research studies from patient recruitment through study completion
• Work directly with study participants, investigators, and pharmaceutical sponsors
• Organize research files, study documentation, and project-related data
• Collect, process, and ship blood, urine, and stool specimens according to protocol
• Perform phlebotomy and assist with patient vital signs
• Complete and maintain Case Report Forms (CRFs) in compliance with FDA and study guidelines
• Enter and verify study data to ensure accuracy, integrity, and protocol compliance
• Maintain regulatory binders and required study documentation
• Manage temperature logs and clinical supply inventory
• Order and distribute dry ice as needed for specimen shipments
• Avoid support subject recruitment efforts through chart reviews, phone outreach, and screening activities
• Schedule and coordinate patient visits
• Perform Fibroscans upon completion of training
• Ensure referring physicians receive appropriate patient participation notifications
• Submit participant stipend and reimbursement requests
• Provide guidance and support to Research Assistants
• Assist with general office and research department operations as needed

Pay

$65,000.00 USD Annually - $80,000.00 USD Annually

Schedule

Monday–Friday
Start Time: Flexible between 7:00 AM – 9:00 AM