Job Title: Research Study Manager

Job Description

We are seeking a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations at our Newark location. This role requires a proactive leader with a strong background in oncology and clinical research coordination.

Responsibilities

• Supervise and manage the workflow of coordinators in the assigned disease-specific group.
• Communicate services that will support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.
• Conduct quality assurance audits to ensure compliance with regulatory standards.
• Partner with physicians to educate and assist them in selecting appropriate studies and explaining feasibility.
• Work with research sites to oversee oncology research and ensure compliance with protocols.
• Assist doctors in selecting trials and understand screening processes to improve site enrollment.

Essential Skills

• Experience in supervising coordinators and managing workflow.
• Prior experience in oncology and as a Clinical Research Coordinator (CRC).
• Strong understanding of clinical operations and regulatory compliance.
• Bachelor’s Degree in a science discipline.
• 3-5 years of oncology experience.
• At least 1 year of supervisory experience.

Additional Skills & Qualifications

• Experience as a Clinical Research Supervisor or Research Program Manager.
• Familiarity with NCI Designated Cancer Institutes.

Job Type & Location

This is a Contract to Hire position based out of New Brunswick, New Jersey.