Jobs at The START Center for Cancer Research

Coordinates multiple early-phase oncology clinical trials under senior research staff guidance. Responsibilities include protocol oversight, sponsor and CRO communication, patient screening and informed consent, source document management, data collection, deviation documentation, adverse event reporting, and trial closeout activities. The role ensures compliance with protocols, SOPs, GCP, regulatory requirements, and patient safety standards while supporting accurate and timely study conduct.

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.

Leads full-cycle recruitment of oncology physicians and physician-investigators across START’s global clinical research network. Develops sourcing strategies, builds talent pipelines, manages candidate relationships, coordinates interviews and site visits, negotiates offers, and supports onboarding. Advises executives on physician workforce planning, labor-market intelligence, recruitment performance, and long-term talent strategy. Cultivates relationships with oncology fellowships, academic cancer centers, principal investigators, and clinical research communities.

Leads onboarding, training, competency development, and operational readiness for clinical research personnel across START’s oncology site network. Develops standardized curricula, delivers virtual and in-person instruction, coaches employees, evaluates competency, coordinates shadowing, and supports new site launches. Partners with cross-functional teams to ensure compliance with SOPs, GCP, regulatory requirements, and operational standards while tracking readiness, training effectiveness, and continuous improvement.

Manages clinical research business operations connecting clinical operations, finance, and revenue cycle teams. Oversees CTMS data accuracy, study-level billing, invoice reconciliation, payment monitoring, discrepancy resolution, KPI reporting, audits, and process improvement. Serves as a liaison among internal stakeholders, sponsors, and CROs to support compliant revenue capture and successful clinical trial execution.

Manages clinical research business operations linking clinical operations and finance. Oversees CTMS data accuracy, reconciliation, sponsor and CRO billing inquiries, invoice disputes, revenue capture, payments, aging accounts, KPIs, audits, and process improvements. Collaborates with clinical, pharmacy, regulatory, finance, and revenue cycle teams to resolve discrepancies, reduce revenue leakage, maintain compliance, and provide reporting to support forecasting and operational decisions.

Supports Clinical Research Coordinators by collecting, de-identifying, entering, transmitting, and resolving queries for clinical trial data. Maintains CTMS records, tracks patient visits and study events, assists with protocol-specific documents, contacts patients for follow-up, supports monitors, and ensures compliance with clinical research regulations and data transmission requirements.

Collects, enters, reviews, corrects, and submits clinical trial data for investigational drug studies. Requests patient records, resolves data queries, maintains current case report forms, coordinates monitor visits and study meetings, reviews protocols, and communicates laboratory information to regulatory staff. The role requires accurate data handling, clinical research documentation, and collaboration with study teams and monitors.

Supervises clinical research coordinators and oversees day-to-day oncology study operations, ensuring compliance with GCP, regulations, SOPs, and quality standards. Responsibilities include staff training and performance assessment, study activation, protocol feasibility reviews, documentation oversight, system and workflow management, process improvement, and collaboration with regulatory, quality, pharmacy, finance, nursing, and other teams. The role supports patient care, recruitment, retention, audit readiness, and effective clinical trial delivery.

Supports clinical research coordinators by collecting, de-identifying, entering, transmitting, and querying clinical trial data. Maintains CTMS records, tracks patient visits and study events, reviews protocols, prepares study documents, supports monitors, coordinates lab information, and communicates with internal teams. The role requires accurate data handling, medical terminology knowledge, protocol understanding, strong organization, and compliance with clinical research regulations.

Provides direct nursing care to oncology clinical-trial participants, including administering chemotherapy, immunotherapy, and investigational agents; performing venipuncture, IV insertion, central-line management, ECGs, vital signs, and specimen collection; educating patients; and coordinating protocol-required procedures with the study team.

Provides direct nursing care to oncology clinical-trial participants, including chemotherapy, immunotherapy, and investigational-agent administration. Performs venipuncture, IV insertion, central-line management, specimen collection, ECGs, and vital signs. Educates patients about clinical-trial participation and treatment side effects, while coordinating protocol-required procedures with the study team.

Schedule clinical trial and patient appointments, radiology procedures, hotel stays, follow-ups, and treatments. Complete prior authorizations, manage referrals, consults, no-shows, patient communications, and electronic medical records. Collaborate with care teams to coordinate quality patient services, apply clinical protocols, support process improvements, and maintain required skills through ongoing education.

Manages clinical activity data integrity across CTMS, EMR, pharmacy, EDC, and financial systems at an oncology clinical research site. Translates clinical documentation into billing and budget constructs, investigates discrepancies, supports sponsor invoice disputes, monitors accounts receivable status, trends data quality metrics, and coordinates with clinical, finance, revenue cycle, and study administration teams. The role also triages patient billing inquiries and escalates compliance, control, and systemic process concerns.

Manages clinical activity data integrity at an oncology research site, ensuring accurate CTMS and FileMaker records, translating clinical documentation into billing data, supporting invoice dispute resolution, monitoring accounts receivable status, and identifying recurring data quality issues. Partners with clinical, finance, revenue cycle, study administration, and quality teams to improve billing accuracy, maintain regulatory controls, and escalate systemic problems. Also triages patient billing inquiries and may travel occasionally to other sites or corporate offices.

Manages clinical activity data integrity at an oncology research site, ensuring accurate CTMS and FileMaker records, clinical-to-billing alignment, invoice support, sponsor dispute resolution, accounts receivable monitoring, KPI trending, and escalation of data or control issues. Coordinates with clinical, finance, revenue cycle, study administration, and quality teams while supporting patient billing inquiries and regulated correction workflows.

Manages clinical activity data integrity at an oncology research site, ensuring accurate CTMS and FileMaker records, clinical-to-billing reconciliation, invoice support, sponsor dispute resolution, and accounts receivable visibility. Coordinates with clinical, finance, revenue cycle, study administration, and quality teams to investigate discrepancies, maintain regulated correction workflows, trend data quality metrics, and improve billing accuracy. Also triages patient billing inquiries and escalates systemic control or compliance concerns.

Supports early-phase oncology clinical trials under senior research staff guidance. Responsibilities include patient education, screening and eligibility assessment, informed consent, protocol and GCP compliance, study coordination, data collection, sponsor and CRO communication, adverse event reporting, and documentation of protocol or SOP deviations. The role involves direct patient interaction and collaboration with principal investigators and clinical research teams.

Leads a deployable Operational Readiness Team supporting new clinical site launches and stabilizing underperforming oncology research sites. Responsibilities include staffing and deployment planning, readiness standards, training, workflow setup, risk monitoring, corrective action plans, compliance alignment, and collaboration with site leaders, investigators, quality teams, and integration leadership. The role requires approximately 50% travel and direct people leadership across a clinical research network.

Leads oncology clinical research study operations, overseeing clinical research coordinators, data coordination, and medical records teams. Ensures compliant, high-quality study conduct, data management, staff training, protocol feasibility, study activation, patient-care workflows, and regulatory adherence. Partners with nursing, quality, regulatory, pharmacy, finance, and shared services teams on process improvement, site operations, and strategic initiatives. Also manages recruitment, retention, supervision, and continuous improvement activities.