Teams at Allina Health

Coordinates clinical research studies from startup through closeout, including participant screening, informed consent, clinical assessments, source documentation, data management, regulatory submissions, feasibility, invoicing, monitoring, audits, and study archiving. Communicates with investigators, sponsors, clinical teams, and research staff while ensuring compliance with protocols, IRB requirements, FDA regulations, SOPs, and ICH GCP guidelines.

Manages clinical research trials and investigator-initiated studies from feasibility and startup through regulatory, contractual, monitoring, and closeout activities. Coordinates IRB submissions, budgets, billing, study documentation, investigational product tracking, and protocol tools. Trains and mentors research and clinical staff, supports compliance with regulatory requirements, and collaborates with research leaders, medical directors, regulatory specialists, and study coordinators across the cancer research program.

Provides comprehensive gynecologic oncology care across outpatient clinics, inpatient rounding, infusion support, sexual health and survivorship visits. Conducts assessments, diagnoses conditions, orders and interprets diagnostics, prescribes treatments, educates patients, and coordinates specialty care. Collaborates with gynecologic oncologists and multidisciplinary teams, supports program development, consults on hospitalized patients, and may perform surgical first-assist duties. New graduates may be considered, while gynecologic oncology or surgical experience is preferred.