Teams at The START Center for Cancer Research

Supports multiple early-phase oncology clinical trials under senior research staff guidance. Responsibilities include coordinating protocol activities, communicating with sponsors and CROs, screening patients, facilitating informed consent, training staff, monitoring protocol compliance, identifying deviations, maintaining accurate documentation, collecting data, and supporting Serious Adverse Event reporting with the Principal Investigator. The role requires adherence to GCP, regulatory requirements, study protocols, and patient safety standards.

Collect, transcribe, and submit clinical trial data into paper and electronic CRFs for investigational drug studies. Review patient records for completeness and accuracy, resolve queries, coordinate monitor visits, identify study labs for regulatory certification, and attend study meetings to support data quality and audit readiness.

Provide leadership and supervision for clinic, infusion, and research nursing teams; ensure staff competency, regulatory compliance (GCP/GDPR), high-quality patient care, training, process improvement, protocol feasibility reviews, CTMS/EHR documentation, and growth in patient referrals and enrollment across oncology clinical research sites.