Clinical Research Coordinator

Arizona Center for Cancer Care•Peoria, AZ

3d•Onsite

About The Position

The Clinical Research Coordinator (CRC) plays a pivotal role in the execution and management of clinical trials and research studies, working closely with principal investigators, research teams, and participants. This position ensures that all processes comply with regulatory, ethical, and organizational standards while contributing directly to the advancement of medical knowledge and patient care.

Requirements

Minimum of 2–3 years of clinical research experience required.
Ability to critically evaluate information and apply problem-solving within healthcare and research settings.
Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
Strong command of medical terminology and effective oral and written communication skills.
Ability to read, write, and communicate effectively in English.
Valid driver’s license and reliable transportation for travel between locations.

Nice To Haves

Associate or bachelor’s degree in biological science, healthcare, or related medical/scientific field preferred.
An equivalent combination of education and relevant experience may be considered.
Experience with electronic data capture systems (e.g., Redcap, Medidata Rave) preferred.

Responsibilities

Collaborates with the Clinical Program Manager and physicians to identify, develop, organize, and implement clinical research activities.
Partners with principal investigators and clinical staff to plan and execute research protocols in compliance with IRB, FDA, and GCP guidelines.
Maintains data integrity and assists in the development of databases for effective data collection and analysis.
Oversee proper storage and accountability of investigational products in accordance with study protocols.
Ensures compliance with all research policies, protocols, and participant protection standards.
Conducts patient recruitment, screening, consenting, and enrollment in compliance with protocol requirements and ethical standards.
Coordinates study visits and procedures, ensuring protocol-specific assessments are scheduled and completed on time.
Tracks and reports adverse events and protocol deviations per regulatory guidelines and sponsor requirements.
Maintains and updates study records in regulatory binders and clinical trial management systems (CTMS), if applicable.
Demonstrates strict confidentiality and discretion in all matters related to research studies and participants.
Apply privacy and safety standards related to job responsibilities and research operations.
Performs other duties as assigned.