Oncology Clinical Trials Coordinator (RN)

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) retirement savings plan with 1:

Annual bonus potential

Paid time off and holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

FSA/HSA options

Collaborative, growth-focused culture

Job summary

The START Center for Cancer Research in Myrtle Beach, SC seeks a Clinical Research Coordinator, RN to support oncology and urology trials under senior staff. Responsibilities include protocol adherence, patient interaction, data collection, and regulatory compliance.

You will monitor trial conduct, train staff, ensure informed consent, and coordinate with investigators to maintain study integrity. Strong GCP knowledge and communication are essential; RN license in-state required.

Qualifications

• Associate’s degree in Nursing required; RN license in state practicing.
• Clinical research experience preferred but not required.
• Strong attention to detail and accuracy in data collection and documentation.
• GCP knowledge and regulatory requirements familiarity.
• Ability to manage multiple tasks in a fast-paced environment.

Responsibilities

• Coordinate daily activities of oncology and urology clinical trials.
• Ensure protocol compliance and patient safety per SOPs and GCP.
• Assist with informed consent, data capture, and source documentation.
• Train staff on protocol requirements and safety procedures.
• Maintain trial files and respond to deviations with leadership.

Skills

RN license

Data collection

Regulatory knowledge

Communication skills

Microsoft Office

Education

Associate’s degree in Nursing

Bachelor’s degree in Nursing

Tools

Clinical trial software

EHR/CTMS systems

Job description

The START Center for Cancer Research in Myrtle Beach, SC seeks a Clinical Research Coordinator, RN to support oncology and urology trials under senior staff. Responsibilities include protocol adherence, patient interaction, data collection, and regulatory compliance.

You will monitor trial conduct, train staff, ensure informed consent, and coordinate with investigators to maintain study integrity. Strong GCP knowledge and communication are essential; RN license in-state required.