Clinical Trial Support Specialist

📋 Description

• Support clinical trial activities across functional areas: patient engagement, study operations
• Educate and communicate with study participants on procedures, visit expectations, follow-ups
• Coordinate participant visits, reminders, transportation, scheduling, attendance tracking, and
• Support patient recruitment and pre-screening via outreach, records review, preliminary
• Maintain accurate information across CTMS, EDC, EMR/EHR, eRegulatory, and other systems.
• Provide regulatory and quality support, including docs, training, submissions, and prep for

🎯 Requirements

• 2–3 years of experience supporting clinical trials, sites, CROs, or sponsors.
• Background in clinical research, medicine, life sciences, nursing, pharmacy, healthcare admin, or
• Current and completed GCP and HIPAA training.
• Familiarity with GCP principles and ICH E6(R3).
• Experience in one or more areas: Clinical Research Coordination, Study Startup, Regulatory Support
• Familiarity with CTMS, EDC, EMR/EHR, eRegulatory platforms, or similar systems.

🎁 Benefits

• Remote work with options for full-time, part-time, or project-based opportunities.
• Opportunities to work with sites, sponsors, CROs, and healthcare organizations across studies.
• Exposure to multiple clinical trial lifecycle areas and opportunities to leverage specialization.
• Flexible engagement depending on study needs.
• Contribution to ethical, scientifically rigorous research supporting new treatments.
• Global, multidisciplinary clinical research support environment.