• Research Study Manager

    Actalent (New Brunswick, NJ)


    Job Title: Research Study ManagerJob Description

     

    We are seeking a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations at the Newark CINJ location. 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.

    Work Environment

    This role is part of an NCI Designated Cancer Institute with a collaborative team of 70 employees, including roles in CRC, Regulatory Affairs, and Clinical Research Management. The work schedule includes three days a week at various sites in locations such as New Brunswick, Tom’s River, Monmouth Med (Lakewood/Long Branch), and Hamilton, with the flexibility of working two days from home. The environment is supportive and focused on advancing cancer research, offering opportunities to work closely with physicians and other healthcare professionals.

     

    Job Type & Location

     

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

    Pay and Benefits

    The pay range for this position is $52.00 - $54.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

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

     

    Workplace Type

     

    This is a hybrid position in New Brunswick,NJ.

     

    Application Deadline

     

    This position is anticipated to close on Oct 20, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.