Clinical Research

• Trial Coordination &amp; Patient Enrollment: Oversee daily study operations, manage pre-screening, validate patient eligibility, and support smooth handoffs to sites for full screening and consent.
• Site Engagement &amp; Communication: Collaborate closely with site staff and investigators to optimize enrollment workflows, support feasibility assessments, and provide study updates.
• Data &amp; Compliance: Ensure accurate data collection, maintain patient confidentiality, and follow GCP, protocol, and regulatory standards.
• Product Feedback &amp; Platform Insights: Capture site-level and patient insights, track issues or improvement opportunities, and work with product/engineering teams to enhance the Paradigm platform, including NLP-driven features.
• Site Visits &amp; Training: Conduct site qualification visits as needed and support onboarding, training, and ongoing guidance for site teams.
• Mentorship &amp; Team Support: Guide junior CRCs, share best practices, and contribute to continuous improvement across the team

Clinical Research Coordinator

Research Finance Specialist II

Oncology Late-Stage Clinical Scientist – Director, Non MD

Clinical Research Assistant

Clinical Research Data Specialist I

Clinical Research Intern