Oncology Clinical Research Coordinator – Early-Phase Trials

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

401(k) matching

Bonuses based on performance

Paid time off & holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA/HSA

Professional growth opportunities

Collaborative, inclusive culture

Job summary

The START Center for Cancer Research in Myrtle Beach, SC is seeking a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will work under senior staff to ensure timely, compliant conduct, with direct patient interaction and data collection, following GCP standards.

Responsibilities include coordinating with sponsors/CROs, monitoring study progress, training staff, screening patients, obtaining informed consent, and assisting with data queries and adverse

Qualifications

• 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.
• 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 with study sponsors/CROs and staff regarding protocol questions and status.
• Monitor day-to-day conduct of studies to ensure protocol, SOP, and GCP compliance.
• Create or revise forms to assure protocol compliance.
• Maintain study files with standardized labeling and filing procedures.
• Train staff on protocol procedures and amendments.
• Screen patients and determine eligibility for trials.
• Facilitate informed consent and manage source documents per SOP.
• Address deviations with leadership and implement corrective actions.
• Assist data coordinators with CRF completion and query resolution.
• Collaborate with the PI to report Serious Adverse Events.
• Support protocol closeout activities with the data coordinator.

Skills

Clinical research

GCP knowledge

Data collection

Communication skills

Patient interaction

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research in Myrtle Beach, SC is seeking a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will work under senior staff to ensure timely, compliant conduct, with direct patient interaction and data collection, following GCP standards.

Responsibilities include coordinating with sponsors/CROs, monitoring study progress, training staff, screening patients, obtaining informed consent, and assisting with data queries and adverse