Jobs at Moffitt Cancer Center

Performs and optimizes pharmacodynamic assays, cell-based drug response studies, immunoassays, molecular biology procedures, and clinical specimen processing. Maintains cell cultures and laboratory instrumentation, troubleshoots automation systems, evaluates assay data, manages quality documentation, and supports investigators in translational research and early-phase clinical studies. The role also assists with assay validation, laboratory operations, inventory management, and training junior personnel.

Performs Medicare and Medicaid reimbursement analysis, including cost reports, contractual allowance and settlement models, reimbursement forecasts, regulatory impact analysis, and Medicaid supplemental program estimates. Maintains cost allocation and physician time-study documentation, coordinates provider enrollment activities, reconciles settlement accounts, and supports reimbursement optimization, financial reporting, and regulatory compliance. Collaborates with government relations, managed care, patient financial services, auditors, and external consultants.

Provides individualized, patient- and family-centered nursing care to cancer patients in a radiation oncology outpatient clinic. Assesses, plans, delivers, documents, and evaluates care; provides patient education and discharge planning; participates in evidence-based improvement and professional development; and collaborates with the multidisciplinary radiation oncology team across Tampa Bay locations.

Provide diagnostic gastrointestinal pathology services including routine sign-out, frozen section coverage, and possible other subspecialty sign-out. Support patient care, translational research, education, and consultative activities as a faculty member at an NCI-designated cancer center.

Coordinate complex patient appointments across multiple resources, gather external records, communicate with stakeholders, and manage follow-up for specialty areas (e.g., biopsies, radiology, bone marrow transplant, infusion/chemotherapy, radiation). Ensure accurate scheduling and stakeholder communication (verbal, written, electronic).

Coordinates oncology clinical trials for myeloma and lymphoma patients under supervision. Responsibilities include screening, enrolling, educating, and monitoring study subjects; coordinating with investigators, medical staff, sponsors, and regulatory teams; maintaining source documentation and study data; reporting adverse experiences; ensuring protocol compliance; and performing administrative research procedures.

Coordinates lymphoma clinical trials by screening, enrolling, educating, and monitoring patients; collaborating with investigators, medical staff, regulatory teams, and sponsors; maintaining protocol-compliant source documentation and study data; reporting adverse experiences; and supporting trial administration under supervision. The role includes paid training and follows a Monday-to-Friday hybrid schedule after an introductory period.

Provides individualized outpatient nursing care to oncology patients and families. Responsibilities include assessing, planning, delivering, documenting, and evaluating care; administering IV fluids, antibiotics, chemotherapy, blood, and platelets; accessing ports and changing central-line dressings; educating patients; supporting evidence-based improvement; and maintaining professional and regulatory standards.

Coordinates clinical trial screening within a gastrointestinal disease program. Identifies potential participants, reviews eligibility, guides patients and caregivers, facilitates referrals, supports enrollment, and helps physicians and research teams follow clinical trial protocols and regulatory requirements. Works with patients, sponsors, and multidisciplinary clinical trial personnel to ensure trials progress safely and efficiently.

Coordinates cancer clinical trials by supporting investigators, screening and enrolling patients, monitoring protocol compliance, documenting study activities, coordinating patient care, and serving as a liaison among investigators, care providers, regulatory staff, and sponsors. The role manages multiple studies, supports complex protocols, follows Good Clinical Practices and human-subject protections, and uses EMR, clinical trial management, and reporting systems.

Oversee biospecimen regulatory compliance and governance for cancer research. Review protocols, consent forms, agreements, and related documentation; develop governance plans, policies, manuals, and procedures; coordinate biospecimen transfers; facilitate review committees; monitor utilization and compliance metrics; train researchers and staff; and support biospecimen projects, workflows, and process improvements.

Manages clinical research data for multiple oncology studies by abstracting information from medical records, entering protocol data into study databases, reviewing case report forms, resolving discrepancies and queries, and supporting monitoring, audits, compliance reviews, and study team activities. The role requires accurate data management, understanding of oncology and medical terminology, adherence to Good Clinical Practice, and collaboration with study coordinators, investigators, sponsors, monitors, and auditors.

Develops and delivers nursing orientation, education, competency programs, and professional development using oncology expertise, adult learning principles, instructional design, and emerging educational technologies. Identifies learning needs and competency gaps, creates educational materials, coordinates programs, and evaluates effectiveness to improve nursing practice and patient outcomes. Requires collaboration with nursing leadership across practice settings, a BSN, Florida RN license, and at least three years of acute care or oncology experience.

Conduct translational cancer research focused on diagnostics, predictive biomarkers, and precision oncology. Design and lead studies, apply histology, immunohistochemistry, spatial proteomics, computational pathology, and genomic profiling, analyze data, publish findings, present at scientific meetings, collaborate across multidisciplinary teams, and develop diagnostic and therapeutic approaches for solid tumors and hematologic malignancies. Supervise and train research staff while preparing protocols and manuscripts under investigator direction.

Coordinates non-therapeutic lymphoma research studies within a hematology clinic. Responsibilities include screening and consenting participants, recruitment and follow-up, specimen collection, data abstraction and entry, protocol compliance, quality assurance, documenting deviations, supporting regulatory submissions, and coordinating with clinical, regulatory, tissue core, and shared-resource teams. The role may also contribute to publications and supports moderate-complexity studies.

Coordinates Protocol Review and Monitoring System committees, including agenda preparation, pre-meeting material review, committee organization, and liaison activities with chairpersons, program leaders, principal investigators, regulatory specialists, and study coordinators. Ensures committee activities support adherence to protocol review, monitoring policies, procedures, and data safety and monitoring requirements.

Negotiate and manage budgets and payment terms for industry, federal, state, and privately funded clinical trials. Ensure budgets comply with institutional policy, fair market value, Medicare coverage, and regulatory requirements. Perform coverage analysis, billing and coding review, and financial forecasting using advanced Excel. Collaborate with PIs, research teams, finance, legal, and sponsors to support efficient trial activation and amendments.

Coordinates non-therapeutic research studies in a hematology clinic, including participant screening, recruitment, consent, follow-up, specimen collection, data abstraction, and database entry. Ensures protocol adherence, data quality, timely deviation documentation, regulatory communication, and coordination with clinical teams and shared resources. Supports study implementation, protocol updates, administrative activities, and potentially research publications.

Designs, configures, tests, implements, and maintains Epic Prelude and related clinical applications. Troubleshoots software/hardware/interfaces, performs QA/integrated testing, develops enhancements and reports, documents builds, mentors junior analysts, and provides 24/7 on-call operational support. Collaborates with clinical and operational teams to align systems with care and operational priorities.

Coordinates clinical trials by supporting principal investigators, screening and enrolling subjects, monitoring protocol compliance, documenting research activities, coordinating patient care, and liaising with investigators, medical staff, regulatory personnel, and sponsors. Manages complex studies with higher patient volumes, develops study procedures, maintains research databases and clinical systems, and ensures adherence to Good Clinical Practices and human-subject protection regulations.