Oncology Clinical Study Operations Lead

START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

401(k) retirement savings plan with EM

Annual performance bonus

Paid time off and holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA plans

Supportive, collaborative workplace

Job summary

The START Center for Cancer Research in Myrtle Beach, SC seeks an experienced leader to oversee the Clinical Research Coordinator team supporting oncology trials. You will ensure quality patient care, drive compliance with GCP and SOPs, and coordinate with cross-functional teams to advance protocol delivery.

Strong leadership, clinical research governance, and proficiency with EHR/CTMS are essential. This role offers a collaborative, fast-paced environment with professional growth opportunities.

Qualifications

• Requires Associate’s degree in health administration, nursing or related field.
• Minimum 5 years clinical research experience and 2 years leadership in oncology.
• CITI GCP training.
• Knowledge of GCP and US federal clinical research regulations.
• Proficient with Microsoft Office and clinical documentation systems.

Responsibilities

• Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team to support patient care and site performance.
• Train, coach, and assess staff competency for assigned responsibilities.
• Ensure timely and accurate study documentation with monitors and auditors and maintain GCP compliance.
• Support study acquisition and activation with Shared Services and protocol review meetings.
• Ensure efficient processes and systems to support patient care and research workflows.
• Identify and implement practical process improvements for patients and site operations.
• Review protocols for operational feasibility focusing on workload and site readiness.
• Coordinate with Regulatory, Quality, Site Development, Pharmacy, Finance and other teams to deliver compliant study delivery.
• Support CTMS, EHR and other systems for accurate data capture in the assigned area.
• Partner with site leaders to address operational issues and improve cross-functional workflows.

Skills

Leadership

GCP knowledge

Regulatory compliance

Microsoft Office

Education

Associate degree

Bachelor/Master degree

Job description

The START Center for Cancer Research in Myrtle Beach, SC seeks an experienced leader to oversee the Clinical Research Coordinator team supporting oncology trials. You will ensure quality patient care, drive compliance with GCP and SOPs, and coordinate with cross-functional teams to advance protocol delivery.

Strong leadership, clinical research governance, and proficiency with EHR/CTMS are essential. This role offers a collaborative, fast-paced environment with professional growth opportunities.