Research Study Manager

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. This role is pivotal in managing the supervision and workflow of coordinators, especially within the oncology field. The ideal candidate will have a strong background in clinical research and a passion for driving the growth and success of clinical studies.

Responsibilities

• Supervise other coordinators and manage workflow effectively.
• Oversee the daily clinical research operations of the Newark CINJ location.
• Supervise and assign tasks within the disease-specific group.
• Communicate services that support and enable the growth of clinical research, focusing on recruitment, retention, coordination, and data management.
• Conduct quality assurance audits to maintain high standards.
• Ensure regulatory compliance across all research activities.
• Partner with physicians to educate and assist them in selecting suitable studies and understanding feasibility.
• Work collaboratively with sites to oversee oncology research, addressing their specific needs and concerns.
• Assist doctors in selecting trials and understanding protocols.
• Encourage site enrollment by developing effective screening processes.

Essential Skills

• Experience in supervising coordinators and managing workflow.
• Prior experience in oncology.
• Proven experience as a Clinical Research Coordinator (CRC).
• 3-5 years of oncology experience.
• At least 1 year of supervisory experience.

Additional Skills & Qualifications

• Bachelor’s degree in a science discipline.
• Familiarity with clinical operations and regulatory compliance.
• Experience in quality assurance audits.
• Ability to communicate effectively with diverse teams and stakeholders.

Job Type & Location

This is a 12-month contract to hire position based out of New Brunswick, New Jersey.