The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START's mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. Learn more at STARTresearch.com.

Join Our Pioneering Team as an Advanced Practice Provider (APP) – Urology and Later Phase Clinical Research Program

The Advanced Practice Provider (APP) – Urology and Later Phase Clinical Research Program supports clinical care and protocol execution for urology-focused and later-phase oncology clinical trials. Operating as a sub-investigator under the supervision of the Principal Investigator (PI), the APP supports patient screening, study visits, and continuity of care while facilitating efficient clinic operations within a disease-focused research environment.

Essential Responsibilities:

• Serve as a sub-investigator on assigned urology and later-phase clinical trials following completion of required training and delegation documentation.
• Conduct protocol-required physical examinations and study visits for patients in screening, on treatment, and in follow-up as delegated by the Principal Investigator.
• Prepare medical histories and clinical summaries in advance of new patient consults to support efficient PI evaluation.
• Assist with patient screening activities, including chart review, protocol feasibility assessment, and coordination of required evaluations.
• Support post-consent screening and ongoing study assessments in accordance with protocol requirements.
• Assist with adverse event (AE) and serious adverse event (SAE) identification, documentation, and follow-up in collaboration with the Principal Investigator and research team.
• Serve as a primary clinical contact for the research care team for routine patient management questions and escalate complex issues to the Principal Investigator.
• Coordinate closely with nursing, clinical research coordinators, and ancillary services to support protocol adherence and patient-centered care.
• Support disease-focused outreach, education, and multidisciplinary collaboration as requested.
• Other duties may be assigned at any time.

Education & Experience:

• Advanced practice degree (Nurse Practitioner or Physician Assistant) with current licensure in the applicable state(s).
• Minimum of 3 to 5 years of experience in urology, oncology, or clinical research.

Preferred Education and Experience:

• Master's degree or Doctoral degree in advanced practice nursing or physician assistant studies.
• National certification as a Nurse Practitioner or Physician Assistant. Eligibility and willingness to serve as a sub-investigator on clinical trials.
• Prior experience in urology clinical care or later-phase oncology clinical research.

Physical & Travel Requirements:

• Travel: Limited travel may be required during training and onboarding.
• Sitting: Must be able to sit for extended periods of time.
• Standing: Must be able to stand for extended periods of time.
• Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks.
• Lifting: Must be able to lift up to 25 pounds.
• Exposure: Works closely with physicians, research staff, and ancillary personnel in caring for and treating urology and oncology patients.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.