Clinical Research RN

Where You’ll Work Hello Humankindness

• Join a Legacy of Healing at Saint Joseph’s Hospital and Medical Center (SJHMC) Ready to make a real difference? Join SJHMC in Phoenix AZ., a 571-bed nonprofit founded by the Sisters of Mercy over 125 years ago. We're more than a hospital; we're a global destination for life-changing care, embracing patients with humankindness. Here, your calling will flourish. We're not just a workplace; we're a community dedicated to a mission of service.
• Leaders in
• Specialized
• Care:
• Barrow
• Neurological
• Institute (BNI): A world-renowned center for groundbreaking neurological research and innovative treatments.
• Norton
• Thoracic
• Institute (NTI): A national leader in advanced thoracic care with pioneering surgical techniques.
• Level
• I
• Trauma
• Center: One of Arizona's busiest ERs, providing immediate, comprehensive care for critically injured patients 24/7. Why SJHMC?
• Culture of
• Excellence &
• Well-being: We care for our people, fostering professional and personal growth.
• Community &
• Collaboration: Be part of a network committed to global health and well-being.
• Join a
• Legacy,
• Shape a
• Future: Over 20% of our patients travel internationally for our specialized care. This is an invitation to join a family of dedicated professionals at the forefront of medical innovation, united by the power of humankindness. Job Summary and Responsibilities As our Clinician Research RN, you will leverage your clinical nursing expertise to critically support and execute clinical research studies, ensuring the highest standards of participant care, data integrity, and compliance within designated research areas.Every day you will actively participate in the lifecycle of clinical trials, which includes identifying and screening potential study participants, providing in-depth education about research protocols, and carefully monitoring participant well-being. Your responsibilities will involve performing essential clinical assessments, accurately collecting and documenting study data, and vigilantly observing for adverse events. To be successful in this role, you will exhibit excellent organizational capabilities, meticulous attention to detail, and a commitment to ethical conduct in research. Your ability to effectively communicate with participants and collaborate within a research team will be key to contributing to meaningful research outcomes. Demonstrates current knowledge of federal and state regulations, guidelines, and policies governing the conduct of clinical trials. Ensures study documents are maintained in compliance with applicable regulations, guidelines and policies (ie- FDA, OHRP, IRB) Complies with licensure, contractual, protocol and policy requirements Directs intradepartmental and external resource activities relating to assigned studies Assists in the review and development of proposed study budgets Ensures compliance with all study billing process requirements Job Requirements Required Bachelor's degree in related field