Clinical Research Coordinator: Trial Ops & Compliance

Arizona Center for Cancer Care; Phoenix (AZ); On-site; USD 55,000 - 85,000; Full time

Job summary

Arizona Center for Cancer Care in Phoenix, AZ is seeking a Clinical Research Coordinator (CRC) to support the execution and management of clinical trials under investigators. The role emphasizes regulatory compliance, data integrity, participant protection, and advancing cancer research.

You will collaborate with physicians and study teams to plan protocols, coordinate visits, oversee data capture systems, recruit and enroll participants, and maintain study documentation with meticulous accuracy.

Qualifications

• Minimum of 2–3 years of clinical research experience required.
• 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.
• 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.

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.

Skills

Clinical research experience

Communication

Critical thinking

Education

Associate or bachelor’s degree in biological science, healthcare, or related medical/scientific field

Tools

Redcap

Medidata Rave

Microsoft Office

Job description

Arizona Center for Cancer Care in Phoenix, AZ is seeking a Clinical Research Coordinator (CRC) to support the execution and management of clinical trials under investigators. The role emphasizes regulatory compliance, data integrity, participant protection, and advancing cancer research.

You will collaborate with physicians and study teams to plan protocols, coordinate visits, oversee data capture systems, recruit and enroll participants, and maintain study documentation with meticulous accuracy.