Research Study Manager

Overview

Supervises oncology research coordinators and manages daily clinical study operations.

Key Responsibilities

• clinical ops
• site screening
• regulatory compliance
• data management
• quality audits
• workflow management

Tasks

-Oversee the daily clinical research operations of the Newark CINJ location. -Partner with physicians to educate and assist them in selecting suitable studies and understanding feasibility. -Encourage site enrollment by developing effective screening processes. -Work collaboratively with sites to oversee oncology research, addressing their specific needs and concerns. -Supervise and assign tasks within the disease-specific group. -Ensure regulatory compliance across all research activities. -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. -Assist doctors in selecting trials and understanding protocols. -Supervise other coordinators and manage workflow effectively.

Requirements

• regulatory
• quality assurance
• supervisory
• oncology
• bachelor's
• clinical coordinator

What You Bring

-Familiarity with clinical operations and regulatory compliance. -Experience in quality assurance audits. -Experience in supervising coordinators and managing workflow. -Ability to communicate effectively with diverse teams and stakeholders. -3-5 years of oncology experience. -Prior experience in oncology. -Bachelor’s degree in a science discipline. -Proven experience as a Clinical Research Coordinator (CRC). -At least 1 year of supervisory experience.

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Benefits

-401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available -Employee Assistance Program -Time Off/Leave (PTO, Vacation or Sick Leave) -Medical, dental & vision -Critical Illness, Accident, and Hospital -Transportation benefits -Short and long-term disability -Health Spending Account (HSA) -Life Insurance (Voluntary Life & AD&D for the employee and dependents)

About Actalent

-Born in July 2021 by merging Aerotek’s engineering & sciences arm with EASi, Actalent emerged as a focused engineering-and-science partner. -Backed by Allegis Group, it drives scale and speed to market via contract, managed, and technical services. -Headquartered in Maryland with global reach, it deploys specialized teams across North America, Europe, and APAC on Fortune 500 projects. -Typical engagements span EV design, vaccine development, lab services, clinical research, and infrastructure systems. -Expertise covers a wide spectrum: aerospace, defense, healthcare, manufacturing, software systems, environmental and civil engineering.

Sector Specialisms