Oncology Clinical Research Coordinator - Early Phase

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 52,000 - 72,000; Full time

Benefits offered by this job

401(k) retirement savings plan with 회사

Job summary

The START Center for Cancer Research in Myrtle Beach, SC, is hiring a Clinical Research Coordinator (CRC) to support early-phase oncology trials under senior staff guidance. You will ensure protocol adherence, data integrity, and patient safety while handling multiple protocols and coordinating patient participation.

Responsibilities include screening, consent, data entry, regulatory compliance, and collaboration with study teams to address protocol questions and adverse event reporting.

Qualifications

• High School Diploma or GED.
• 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Responsibilities

• Communicate with Study Sponsor, CRO staff regarding questions, concerns, and protocol status.
• Monitor day-to-day conduct of studies per protocol requirements and GCP.
• Create or revise forms to assure protocol compliance.
• Maintain files with standardized labeling and filing procedures.
• Implement initial protocol and amendments and train involved staff.
• Assist with patient screening and eligibility determinations.
• Facilitate the informed consent process.
• Identify protocol deviations and coordinate corrective actions.
• Assist data coordinator with case report forms and query resolution.
• Collaborate with Principal Investigator to complete Serious Adverse Event reports.

Skills

Attention to detail

GCP knowledge

Data collection

Microsoft Office

Education

High School Diploma or GED

Tools

Clinical trial management software

Microsoft Office Suite

Job description

The START Center for Cancer Research in Myrtle Beach, SC, is hiring a Clinical Research Coordinator (CRC) to support early-phase oncology trials under senior staff guidance. You will ensure protocol adherence, data integrity, and patient safety while handling multiple protocols and coordinating patient participation.

Responsibilities include screening, consent, data entry, regulatory compliance, and collaboration with study teams to address protocol questions and adverse event reporting.