Remote Clinical Trial Support Specialist (Multiple Openings)
Remote · United States
Job Summary
Remote Clinical Trial Support Specialist handling a multi-disciplinary set of functions across clinical trial lifecycle. Roles include patient education and engagement, visit scheduling and coordination, patient recruitment and pre-screening, regulatory support, data entry and source management, QA and compliance, contract/budget support, sponsor/CRO relations, reimbursement coordination, financial/bookkeeping tasks, and telehealth/decentralized trial coordination. Candidates typically have 2-3 years in clinical research or healthcare operations, a medical/biopharmaceutical or life sciences background with GCP and HIPAA training, experience with CTMS/EDC/EMR/EHR or related platforms, strong communication skills, multilingual capabilities, and the ability to work remotely. Requirements emphasize identifying functional areas that match experience, providing references, and availability (Full-Time, Part-Time, or Project-Based). The role supports remote study activities, virtual site coordination, and cross-functional operational support for sponsors, CROs, and research sites.
Required Qualifications
- 2-3 years experience in clinical research or healthcare operations
- Medical/biopharmaceutical background or life sciences degree
- Completed and current GCP and HIPAA training
- Familiarity with CTMS, EDC, EMR/EHR, eRegulatory systems
- Strong organizational and documentation skills
- Excellent English written and verbal communication
- Ability to work independently in a remote environment
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