Jobs at The START Center for Cancer Research

Support daily conduct of early-phase oncology clinical trials: screen and consent patients, manage source documents and protocol compliance, coordinate with sponsors/CROs, assist data entry and SAE reporting, implement protocol/amendments, and ensure adherence to GCP and SOPs.

Provide direct infusion nursing care to clinical trial participants: administer chemotherapy/immunotherapy/investigational agents, perform venipuncture/IV and central line management, collect specimens and ECGs, record protocol data, educate patients, coordinate with study team and ensure study procedures and documentation meet protocols and EHR/PQRS quality standards.

Provide nursing care and triage to oncology clinical trial participants: perform telephone triage, patient education on investigational therapies, document history in the EMR, coordinate care, assist with prescription refills and EHR quality standards.

Provide protocol-compliant clinical care and support execution of Phase I and early-phase oncology trials as a sub-investigator. Conduct physical exams, screening, study visits, AE/SAE documentation, care coordination, and collaborate with PI, nursing, pharmacy, and research teams to ensure safe, protocol-adherent patient management.

Support day-to-day conduct of early‑phase oncology clinical trials: screen patients, facilitate informed consent, collect and document data, maintain regulatory files, communicate with sponsors/CROs, assist with CRF completion, SAE reporting, and protocol closeout while ensuring GCP compliance and patient safety.

Support daily operations of early‑phase oncology clinical trials: screen and consent patients, collect and manage source data, ensure protocol and GCP compliance, communicate with sponsors/CROs, assist with SAE reporting and study closeout.

Provide nursing support for oncology clinical trial participants: telephone triage, patient education, vital signs/ECGs, basic exams, coordinate care, obtain labs, complete preauthorization paperwork, and assist physicians with trial assessments.

Prepare and submit regulatory documents (IRB, FDA, IBC) for oncology clinical studies, draft informed consents, maintain Investigator Site Files, act as point of contact with Sponsors/CROs and regulatory bodies, track activities in regulatory systems, and respond to inquiries and status requests.

Support daily operations of early-phase oncology clinical trials: screen patients, obtain informed consent, collect and document data per protocol and GCP, coordinate with sponsors/CROs, assist with CRFs, SAE reporting, and protocol implementation.

Provide direct infusion nursing care for oncology clinical trial participants: administer chemotherapy/immunotherapy/investigational agents, perform venipuncture and IV/central line management, collect samples and vitals, educate patients on trials and side effects, coordinate protocol-related procedures, and document per SOPs and EHR.

Coordinate day-to-day conduct of early‑phase oncology clinical trials: screen patients, facilitate informed consent, collect and document data, educate patients on treatments/side effects, report serious adverse events, communicate with sponsors/CROs, and ensure GCP and regulatory compliance.

Lead and oversee genitourinary oncology clinical trials (including Phase 1), ensuring protocol execution, patient safety, data integrity, sponsor relations, regulatory compliance, team leadership, and strategies for patient recruitment and trial growth.

Lead nursing and clinical research operations for an oncology site network, overseeing coordinators, nurses, and scheduling teams. Ensure compliant study conduct, data accuracy, CTMS/EHR implementation, protocol feasibility reviews, process improvement, and cross-department collaboration to support study growth and patient-centered care.

Lead nursing and clinical research operations for an oncology site, overseeing coordinators, nurses, and support teams. Ensure compliant study conduct, manage CTMS/EHR implementation, drive process improvements, support protocol feasibility, and collaborate with quality, regulatory, and investigators to meet enrollment and operational goals.

Coordinate and manage study-specific patient scheduling (appointments, radiology, procedures, hotel stays), complete prior authorizations, handle referrals and no-shows, maintain electronic medical records, answer calls, and collaborate with clinic team to ensure coordinated, high-quality care and continuous improvement.

Provide protocol-compliant clinical care and support execution of Phase I and early-phase oncology trials as a sub-investigator. Conduct study visits, physical exams, screening, AE/SAE identification and documentation, care coordination, and collaborate with PI, nursing, pharmacy, and research staff to ensure safe, protocol-adherent patient management.

Lead and oversee clinical research operations for oncology early‑phase trials, managing CRC, data, and medical records teams. Ensure GCP and regulatory compliance, timely data management in Veeva/CTMS/EHR, support study startup/activation, drive process improvements, cross‑department collaboration, training, SOP/QMS adherence, and site operational leadership.

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.

Support daily conduct of early-phase oncology clinical trials: screen and consent patients, collect and manage source data, ensure protocol and GCP compliance, coordinate with sponsors/CROs, assist with SAE reporting and closeouts, train staff, perform patient triage and education, and maintain study documentation.

Temporary role to clean up and update clinical trial documentation: manage ISFs, eBinders, version control, training records, delegation logs, and OnCore tasks. Ensure regulatory compliance with GCP and collaborate with research teams, monitors, and departments to support study start-up, maintenance, close-out, and audits.