Travel Clinical Research Coordinator & Site Feasibility

CovarsaDx corporation.; United States; Remote; USD 70,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) plan with company match

Paid time off, sick pay, and holiday

Job summary

CovarsaDx is seeking a Travel Clinical Research Coordinator / Site Identification Associate to support clinical trial execution at assigned investigative sites across the United States. The role combines on-site study coordination with secondary site identification and feasibility duties when travel demand is lower.

You will assist principal investigators, site staff, and internal teams with start-up, enrollment, visit coordination, data entry, and regulatory documentation while ensuring GCP

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 2+ years clinical research experience.
• Knowledge of GCP, informed consent processes, source documentation and regulatory docs.
• Willingness to travel frequently (up to 70%).
• Experience with study start-up, enrollment, data entry, site communication.

Responsibilities

• Travel to assigned clinical research sites to provide on-site study coordination support.
• Assist investigators, site staff, and internal teams with study start-up and ongoing conduct.
• Support participant screening, enrollment, visit coordination, and follow-up per protocol.
• Assist with source documents, CRFs, data entry, and query resolution.

Skills

Clinical research experience

Travel readiness

MS 365

EDC systems

Site coordination

Education

Bachelor’s degree in Life Sciences or related

Tools

Microsoft 365

Clinical trial tracking tools

Job description

CovarsaDx is seeking a Travel Clinical Research Coordinator / Site Identification Associate to support clinical trial execution at assigned investigative sites across the United States. The role combines on-site study coordination with secondary site identification and feasibility duties when travel demand is lower.

You will assist principal investigators, site staff, and internal teams with start-up, enrollment, visit coordination, data entry, and regulatory documentation while ensuring GCP