Oncology Clinical Research Coordinator, Early-Phase Trials

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) match

Annual bonus

PTO & holidays

Medical coverage

Life & disability

EAP program

FSA/HSA benefits

Inclusive culture

Job summary

The START Center for Cancer Research in Myrtle Beach is seeking a Clinical Research Coordinator (CRC) to support daily activities of early-phase oncology trials. Under supervision of senior staff, you will ensure accurate and timely conduct of studies, adherence to GCP, and patient safety while coordinating data collection and protocol-specific tasks.

Responsibilities include coordinating patient participation, obtaining informed consent, maintaining study files, communicating with sponsors and

Qualifications

• High School Diploma or GED required.
• 2 years of clinical research experience preferred.
• Basic understanding of oncology clinical trials, particularly Phase 1.
• 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.

Responsibilities

• Communicate regularly with Sponsors, CROs, staff, and others regarding protocol status and questions.
• Monitor day-to-day conduct of studies to ensure adherence to protocol, SOPs, and GCP.
• Create or review forms to ensure protocol compliance.
• Maintain study files with standardized labeling and filing.
• Implement initial protocol and amendments; train staff involved in patient treatment.
• Assist with patient screening and eligibility determination.
• Facilitate informed consent processes and ensure proper completion.
• Prepare and manage source documents per SOPs.
• Identify protocol deviations and coordinate corrective actions.
• Assist data coordinators with case report forms and query resolution.
• Work with the Principal Investigator to document Serious Adverse Events.
• Closeout activities for protocols in coordination with data staff.
• Provide documentation for deviations and SOP adherence.
• Ensure all team members understand and follow assigned protocols.
• Other duties as assigned.

Skills

Attention to detail

Time management

Communication skills

GCP knowledge

Microsoft Office

Education

High School Diploma or GED

Tools

Clinical trial management software

MS Office

Job description

The START Center for Cancer Research in Myrtle Beach is seeking a Clinical Research Coordinator (CRC) to support daily activities of early-phase oncology trials. Under supervision of senior staff, you will ensure accurate and timely conduct of studies, adherence to GCP, and patient safety while coordinating data collection and protocol-specific tasks.

Responsibilities include coordinating patient participation, obtaining informed consent, maintaining study files, communicating with sponsors and