Advanced Practice Provider - Hematology Medicine - Full Time

University of Miami•Miami, FL

10d

About The Position

The Advanced Practice Provider provides clinical care to patients participating in hematology clinical trials, independently and in collaboration with physician investigators. The role supports patient screening, enrollment, treatment, and ongoing study participation while ensuring high-quality, protocol-compliant care. It contributes to the design, implementation, conduct, and evaluation of Phase I–III, investigator-initiated, and industry-sponsored clinical research studies. The position serves as a clinical research sub-investigator and collaborates with principal investigators, research coordinators, sponsors, investigational pharmacy, and multidisciplinary teams. It supports study activation, implementation, enrollment, and conduct while maintaining participant safety, accurate documentation, data integrity, and audit readiness. The role also contributes to protocol development, quality improvement, scholarly dissemination, research mentorship, and initiatives advancing cancer care, supportive care, survivorship, and clinical research. The position requires a master’s degree or higher, an applicable Florida APRN or PA license and board certification, and at least two years of relevant advanced practice experience. The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission, and more.

Requirements

Master’s degree or higher.
Florida APRN or PA license.
Graduate of a master’s in science of nursing or higher curriculum.
For APRNs, board certification from a nationally accredited organization such as ANCC or AANP; for PAs, board certification from NCCPA.
Current BLS and ACLS certification.
CITI certification within one month of employment and ongoing maintenance of CITI certification.
ONS Chemotherapy and Biotherapy certification on hire or during orientation.
Minimum two years of relevant advanced practice experience.
Ability and motivation to work independently in a role with significant autonomy.
Maintain national certification.
Ability to learn new procedures, technologies, and protocols and adapt to changing priorities and work demands.
Ability to work collaboratively and contribute to a team environment.
Technical proficiency with office software, technology, and relevant computer applications.
Strong written and verbal communication skills.

Nice To Haves

Doctorate of Nursing Practice or Science.
Research background or experience.
Two years of experience for hematology/oncology positions.
AOCNP certification within one year of employment.
Ability to author or contribute to an abstract, poster, article, or protocol.

Responsibilities

Conduct and document study-specific assessments, physical examinations, and health histories in accordance with clinical trial protocols.
Evaluate research participants for study eligibility, treatment response, toxicity management, and ongoing protocol participation.
Order, perform, and interpret protocol-required diagnostic and therapeutic tests in collaboration with the research team and principal investigator.
Prescribe and manage study-related and supportive care interventions consistent with protocol requirements, scope of practice, and participant needs.
Monitor participant safety, identify adverse events, and implement interventions to maintain physiologic stability and protocol compliance.
Assess, document, and facilitate timely reporting of adverse events, serious adverse events, protocol deviations, and unanticipated problems in accordance with applicable requirements.
Serve as a clinical research sub-investigator for Phase I, II, and III, investigator-initiated, and industry-sponsored clinical trials.
Collaborate with principal investigators, research coordinators, sponsors, and multidisciplinary teams on study activation, implementation, enrollment, and conduct.
Ensure compliance with Good Clinical Practice, Institutional Review Board requirements, sponsor guidelines, and applicable regulatory standards.
Participate in sponsor monitoring visits, audits, inspections, and regulatory reviews, ensuring documentation, source records, and clinical activities are audit-ready.
Maintain accurate, timely, and complete research documentation, source records, and study-related clinical data.
Collaborate with investigational pharmacy and study teams to ensure safe administration, handling, accountability, and monitoring of investigational agents.
Educate research participants, families, and healthcare professionals about study procedures, treatment plans, risks, benefits, and participation requirements.
Contribute to protocol development, quality improvement initiatives, scholarly dissemination, and clinical and translational research.
Provide research mentorship and guidance to research coordinators, nurses, advanced practice providers, and other study team members.
Co-lead investigator-initiated research, quality improvement, and evidence-based practice initiatives advancing cancer care, supportive care, survivorship, and clinical research.
Adhere to University and unit-level policies and procedures and safeguard University assets.
Participate in the 360 peer review process, submit annual protocols to the practice site, maintain national certification and CITI certification, and contribute to an abstract, poster, article, or protocol.