Lead Oncology Research Coordinators

The START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

401(k) with match

Annual bonus

Paid time off

Medical coverage

Life insurance

EAP

Job summary

The START Center for Cancer Research in Myrtle Beach, SC is seeking a Supervisor of Research Coordinators to lead the clinical research coordinator team and ensure study conduct aligns with START standards and regulatory requirements. The role oversees patient care quality, study activation, and department processes.

Responsibilities include training staff, coordinating with nursing, data coordination, and Shared Services, and driving process improvements while maintaining compliant

Qualifications

• Associate’s degree in health administration, nursing or other related field.
• Minimum 5 years clinical research experience plus 2 years of leadership experience in an oncology clinical research setting.
• CITI GCP training.
• Knowledge of GCP and applicable federal clinical research regulations in the United States.
• Must be familiar with Microsoft Office applications and clinical documentation systems.

Responsibilities

• Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team to support quality patient care and achievement of site-specific performance expectations.
• Train, coach, and assess staff competency for assigned job responsibilities.
• Ensure timely and accurate study documentation and communication with monitors and auditors. Maintain compliance with GCP, applicable SOPs, and required training documentation.
• Support study acquisition and activation in partnership with Shared Services, including participation in protocol review meetings and oversight of accurate site-level data collection and documentation in required systems.
• Ensure efficient and compliant processes and systems are used to support patient care and clinical research workflows
• Identify and implement practical process improvements that support patients, staff, and site operations.
• Review incoming protocols for operational feasibility, with a focus on Clinical Research Coordinator workload, workflow, and site readiness.
• Coordinate with Regulatory, Quality, Site Development, Pharmacy, Finance, and other support teams to promote compliant and effective study delivery
• Support effective use of the CTMS, EHR, and other required systems to ensure accurate documentation and data capture within the assigned area.
• Partner with site and department leaders to address operational issues and improve cross-functional workflows.
• Other duties may be assigned at any time.

Skills

Leadership

Regulatory compliance

Communication

Education

Associate degree in health administration or related field

Bachelor's/Master's degree in health administration or related field

Tools

Microsoft Office

Clinical documentation systems

Job description

The START Center for Cancer Research in Myrtle Beach, SC is seeking a Supervisor of Research Coordinators to lead the clinical research coordinator team and ensure study conduct aligns with START standards and regulatory requirements. The role oversees patient care quality, study activation, and department processes.

Responsibilities include training staff, coordinating with nursing, data coordination, and Shared Services, and driving process improvements while maintaining compliant