Director, Study Operations — Oncology Trials Leader

START Center for Cancer Research; New York (NY); On-site; USD 145,000 - 155,000; Full time

Benefits offered by this job

401(k) retirement plan

Annual performance bonus

Generous paid time off

Medical, dental, vision coverage

Life and disability insurance

Employee Assistance Program

Flexible FSA/HSA

Collaborative work environment

Job summary

The START Center for Cancer Research in Manhattan, NY seeks a Director of Study Operations to lead research operations, overseeing Clinical Research Coordinators, Data Coordinators and Medical Records with autonomy. You will collaborate across departments to ensure GCP-compliant, high-quality patient care and efficient study start-up and activation.

Required are a Bachelor’s degree and 5 years of leadership in oncology clinical research, with GCP/GDPR knowledge and MS Office proficiency.

Qualifications

• Bachelor’s degree required with at least 5 years in oncology clinical research leadership.
• GCP training and knowledge of GDPR and US federal regulations are required.
• Proficiency with Microsoft Office and clinical documentation systems.

Responsibilities

• Lead Clinical Research Coordinator, Data Coordination and Medical Records teams.
• Ensure data management, monitoring communications, and regulatory compliance.
• Support study acquisition/activation with global shared services to speed start-up.
• Collaborate with nursing and shared services for site operations and QA.
• Drive process improvement and inter-departmental collaboration.

Skills

Leadership

GCP knowledge

Regulatory compliance

Communication

Education

Bachelor’s degree

Master’s degree preferred

Tools

Veeva

Microsoft Office

Job description

The START Center for Cancer Research in Manhattan, NY seeks a Director of Study Operations to lead research operations, overseeing Clinical Research Coordinators, Data Coordinators and Medical Records with autonomy. You will collaborate across departments to ensure GCP-compliant, high-quality patient care and efficient study start-up and activation.

Required are a Bachelor’s degree and 5 years of leadership in oncology clinical research, with GCP/GDPR knowledge and MS Office proficiency.