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 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.

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 front-desk and administrative support for a clinical research site: answer calls, greet visitors, manage filing and records, schedule travel and meetings, prepare agendas and minutes, maintain office supplies and petty cash, and resolve administrative inquiries to ensure smooth operations.

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.

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.

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.

Develop, implement, and maintain clinical trial budgets and financial guidelines. Review protocols, perform coverage analysis, prepare and negotiate budgets and contract payment terms, and coordinate with clinical teams and sponsors to ensure billing compliance.

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 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.

Provide direct infusion nursing care for clinical trial participants: administer chemotherapy/immunotherapy/investigational agents, perform venipuncture/IV insertion and central line management, collect vitals and ECGs, educate patients, and coordinate protocol-related procedures with the study team.

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.

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.

Lead nursing and clinical research operations across multiple teams, ensuring compliant, high-quality patient care and study conduct. Oversee referral intake, scheduling, CTMS/EHR implementation, data capture, SOPs, and protocol feasibility. Serve as liaison to investigators and cross-functional partners, drive process improvements, track enrollment metrics, and support site activation, compliance (GCP, GDPR), and staff development.

Lead nursing and clinical research operations across START sites, overseeing coordinators, nurses, and support teams. Ensure compliant study conduct, implement EHR/CTMS, support study startup and feasibility, drive process improvements, track operational metrics, and collaborate with quality, regulatory, pharmacy, and investigators to support patient-centered oncology trial delivery.

Lead and oversee nursing and clinical research operations across referral intake, scheduling, study startup, and patient navigation. Manage and develop multidisciplinary teams, implement CTMS/EHR workflows, ensure GCP/GDPR compliance, support protocol feasibility and study allocation, and drive continuous improvement and cross-functional collaboration to meet study and patient-care goals.

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 CRF completion, SAE reporting, and protocol closeouts while maintaining documentation and regulatory requirements.

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.

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.