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Clinical Research Study Manager
Clinical Research Study ManagerNew Jersey Staffing • New Brunswick, NJ, US
Clinical Research Study Manager

Clinical Research Study Manager

New Jersey Staffing • New Brunswick, NJ, US
Hace 4 días
Tipo de contrato
  • Temporal
Descripción del trabajo

Research Study Manager

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 include :

  • 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 include :

  • 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 and qualifications include :

  • 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.

    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 : Medical, dental & vision; Critical Illness, Accident, and Hospital; 401(k) Retirement Plan; Life Insurance; 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 29, 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.

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    Clinical Research Manager • New Brunswick, NJ, US

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