Paradigm is rebuilding the clinical research ecosystem by enabling equitable access to trials for all patients. Our platform enhances trial efficiency and reduces the barriers to participation for healthcare providers.
Requirements
- 3–5+ years of CRC experience, preferably in a startup or tech-forward clinical research environment
- Strong patient-facing clinical trial experience, including recruitment, enrollment, and pre-screening.
- Proven ability to communicate with site teams, investigators, and cross-functional stakeholders.
- Comfort providing structured feedback to technical teams and collaborating to improve workflows and product features.
- Oncology clinical trial experience.
Responsibilities
- Oversee daily study operations, manage pre-screening, validate patient eligibility, and support smooth handoffs to sites for full screening and consent.
- Collaborate closely with site staff and investigators to optimize enrollment workflows, support feasibility assessments, and provide study updates.
- Ensure accurate data collection, maintain patient confidentiality, and follow GCP, protocol, and regulatory standards.
- 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.
- Conduct site qualification visits as needed and support onboarding, training, and ongoing guidance for site teams.
- Guide junior CRCs, share best practices, and contribute to continuous improvement across the team
Other
- Excellent organizational, problem-solving, and communication skills.
