Clinical Research Supervisor
Core
Oversees clinical research operations, patient workflows, and data infrastructure for early cancer detection and molecular residual disease monitoring programs.
Role type
Senior Clinical Research Supervisor (Program Management)
Builds
Clinical research operations and patient-facing workflows for early cancer detection technologies
Domain
Oncology / Clinical Research / Healthcare
Required skills
Clinical research operations management, Study workflow oversight, Data quality management, Regulatory compliance, Team leadership, SOP development
Preferred skills
Oncology trial experience, Medical terminology, CTCAE knowledge, REDCap/EDC proficiency, Clinical Research Professional certification
Technologies
REDCap, EDC, ctDNA reporting systems
Responsibilities
Support day-to-day SHERLOCK and Gilgan clinical research operations including patient referral, screening, consent, specimen collection, tracking, and follow-up; Oversee study workflows, data systems, and operational performance metrics; Coordinate ctDNA reporting and vendor relationships; Identify operational challenges and implement process improvements; Provide guidance, onboarding, training, and mentoring for research trainees; Develop and maintain SOPs and operational documentation; Support recruitment, audit readiness, and regulatory compliance.
Seniority
Senior, hands-on IC with leadership responsibilities