Research Coordinator - Clinical-Only Local Candidates-Glendale

Ironwood Cancer and Research Centers•Glendale, AZ

4d•Onsite

About The Position

Ironwood Cancer & Research Centers is seeking a qualified, experienced Research Coordinator to manage and coordinate all clinical-trial activities at Ironwood Physicians, PC facilities, including clinical and administrative/regulatory work. The role requires in-depth knowledge of protocol requirements and ensures studies are conducted in accordance with protocol guidelines, departmental standards, good clinical practices, federal regulations, and international guidelines. This is a full-time, Monday-through-Friday day-shift position at the Glendale location. Relocation assistance is not available; candidates must live within commuting distance or relocate independently and be prepared to begin within 2–4 weeks of receiving an offer. The Research Coordinator works with investigators, study staff, primary care providers, IRBs, sponsors, and research nurses to coordinate study feasibility, participant recruitment and follow-up, protocol compliance, study documentation, and required patient procedures. Ironwood Cancer & Research Centers provides comprehensive cancer care through a multidisciplinary team and states its mission is to serve the community with quality, comprehensive cancer care that respects each individual's values and needs.

Requirements

Associate or bachelor's degree.
Clinical experience in oncology or other acute care.
Prior research experience.
Prior phlebotomy experience.
Excellent clinical and functional skills.
Organized and detail-oriented.
Proficiency in Microsoft Office, Word, Outlook, and the Internet.
Ability to use office equipment and a computer.

Nice To Haves

Data-entry experience.
Current IATA training.
Human subjects protection training.
Good Clinical Practice (GCP) training.

Responsibilities

Act as liaison between investigators, other study staff, primary care providers, the IRB, and sponsors.
Review studies for clinical and operational feasibility with the Investigator and Director of Research.
Screen, consent, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while subjects are on study, with Research Nurses' oversight for clinical decision-making support.
Maintain data and source documentation, report adverse experiences, and assist the Regulatory Specialist with maintaining complete regulatory files.
Develop screening, enrollment, and follow-up mechanisms.
Ensure randomization and blinding procedures, as applicable, are followed according to protocol guidelines.
Schedule and perform protocol-required patient procedures, assessments, evaluations, and testing, including blood sample collection, processing and shipping, ECGs, and vital signs, as applicable.