Job Description
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 10,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time's Top Workplaces. A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001. Summary Nurse Practitioner / Physician Assistant -
Early Therapeutics Position Highlights :
Assists physicians and principal investigators with the evaluation, management, and treatment of a broad spectrum of patients participating in early-phase clinical trials, primarily in solid tumor oncology, with exposure to diverse therapeutic modalities (e.g., targeted therapies, immunotherapies, cellular therapies, etc.) Works within a defined scope of practice and under the authority of supervising physician(s), study investigators, and/or specific clinical trial protocols. Plays a key role in the delivery of cutting-edge investigational therapies within a dedicated Clinical Research Unit, ensuring patient safety, protocol compliance, and high-quality clinical care. Engages in a highly collaborative, academic environment with opportunities to contribute to innovative cancer research and advancement of new therapeutics. Responsibilities:
Provides comprehensive patient care as a member of an interdisciplinary clinical and research team, collaborating closely with oncologists, research nurses, pharmacists, and other specialists to coordinate and optimize care for patients enrolled in clinical trials. Performs detailed clinical assessments, including history and physical examinations, with an emphasis on identifying eligibility, toxicity, and response in accordance with study protocols. Correlates subjective and objective data to formulate differential or working diagnoses, particularly in the context of complex oncology patients and investigational treatments. Formulates and implements treatment and management plans for medical conditions and treatment-related toxicities within scope of practice and protocol requirements. Monitors and manages adverse events, including immune-related and novel therapy-associated toxicities, ensuring timely reporting and adherence to regulatory and protocol guidelines. May perform minor procedures within scope of practice, as required for patient care and protocol-specific assessments. Prescribes oral and intravenous medications, including supportive care therapies and protocol-directed treatments, within scope of practice. Ensures accurate, timely, and protocol-compliant documentation of patient care, adverse events, and clinical outcomes in the medical record and research systems. Participates in patient education regarding clinical trial participation, investigational therapies, potential risks, and expected outcomes. Supports screening, enrollment, and retention of patients in clinical trials, contributing to the successful execution of early-phase research studies. Credentials and Qualifications:
Bachelor's degree at minimum; Master's or Doctorate degree preferred. Graduate of an accredited Advanced Registered Nurse Practitioner (APRN) or Physician Assistant (PA) program. Active ACLS and BLS certification required. Prior experience in oncology, clinical research, critical care, and/or internal medicine strongly preferred. Experience with early-phase (Phase I/II) clinical trials or investigational therapeutics is highly desirable. Demonstrated ability to work in a fast-paced, highly collaborative, and protocol-driven environment with strong attention to detail and patient safety.
