Oncology CRC — Early-Phase Clinical Research Coordinator

The START Center for Cancer Research; West Valley City (UT); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) retirement savings plan withem-

Annual performance bonus

Generous paid time off and holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA plans

Supportive, balanced work environment

Collaborative, innovative workplace

Job summary

The START Center for Cancer Research seeks a Clinical Research Coordinator (CRC) to support daily activities of early phase oncology clinical trials. You will work under senior staff to ensure accurate, timely conduct in accordance with protocols, GCP, and patient safety standards.

The role involves direct patient interaction, data collection, and protocol-specific responsibilities. This position requires attention to detail, multitasking, and effective communication with sponsors, CROs, and

Qualifications

• High School Diploma or GED is required.
• At least 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, esp. Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Excellent organizational and time-management skills.
• Strong communication skills, both written and verbal.
• Ability to interact professionally with patients, study staff, and external stakeholders.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Responsibilities

• Communicate regularly with Sponsors, CROs, staff, and others regarding protocol status.
• Monitor day-to-day conduct of studies per protocol requirements and GCP to ensure integrity.
• Create/review forms to assure protocol compliance.
• Maintain files using standardized labeling and filing procedures.
• Implement protocol and amendments, training staff involved in patient care.
• Maintain an up-to-date contact list for study stakeholders.
• Assist with patient screening and eligibility determinations.
• Facilitate informed consent processes to ensure proper completion.
• Prepare/manage source documents per SOPs.
• Identify protocol deviations and coordinate corrective actions.
• Assist data coordinator team with case report form completion and queries.
• Collaborate with Principal Investigator to complete and submit SAE reports.
• Perform protocol-specific closeout activities with data coordination.
• Provide documentation for all deviations to protocols or SOPs.

Skills

Communication

Attention to detail

Time management

Multitasking

Team collaboration

Regulatory understanding

Education

High School Diploma or GED

2 years clinical research experience

GCP knowledge

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research seeks a Clinical Research Coordinator (CRC) to support daily activities of early phase oncology clinical trials. You will work under senior staff to ensure accurate, timely conduct in accordance with protocols, GCP, and patient safety standards.

The role involves direct patient interaction, data collection, and protocol-specific responsibilities. This position requires attention to detail, multitasking, and effective communication with sponsors, CROs, and