Remote Clinical Trial Support Specialist

About the role

We are looking for remote Clinical Trial Support Specialists to join Angel City VA’s virtual research support platform. In this role you will assist independent clinical sites, sponsors and CROs across the full lifecycle of clinical studies, ensuring high‑quality patient engagement and regulatory compliance.

Key responsibilities

• Guide trial participants through study procedures, visit expectations and consent processes.
• Deliver patient education initiatives and support retention strategies.
• Provide regulatory assistance, including GCP and HIPAA compliance documentation.
• Assist study operations teams with data entry, scheduling, and sponsor communications.
• Support finance, administration and sponsor‑relation tasks as needed.

Required profile

• 2‑3 years of experience in medical or biopharmaceutical settings.
• Completed and current GCP and HIPAA training.
• Ability to indicate functional expertise (patient engagement, regulatory support, study operations, etc.) in application.
• Willingness to provide three professional references and undergo background checks.

Required skills

• GCP training
• HIPAA training

What we offer

• Full‑time, part‑time and project‑based remote opportunities.
• Access to a global pipeline of clinical research projects.
• Collaborative, fast‑paced virtual work environment.