Job Title: QA SpecialistJob Description

The Quality Assurance Specialist is tasked with conducting quality assurance audits of research protocols and operations to ensure compliance with FDA, GCP, ICH guidelines, and internal standard operating procedures. The role involves reviewing and analyzing documents, monitoring research and administrative activities, and educating Investigators and research staff. Additionally, the specialist will support the development of center initiatives in quality assurance and data monitoring to enhance clinical research services.

ResponsibilitiesConduct quality assurance audits to ensure compliance with FDA, GCP, ICH guidelines, and internal SOPs.Review and analyze research documents and monitor activities.Provide education to Investigators and research staff.Support the development of quality assurance and data monitoring initiatives.Facilitate clinical research services to achieve overall quality research objectives.Essential SkillsExperience with basic medical terminology.Ability to ensure accuracy between medical records and CRF.Experience working with research protocols.Additional Skills & QualificationsBachelor's Degree in a related field, Master's Degree preferred.Minimum of one year of experience in oncology clinical trials research in an academic, pharmaceutical, or governmental setting.Experience in quality assurance and data monitoring.Hands-on auditing experience in a government and/or pharmaceutical industry setting.Knowledge of United States Federal regulations and Medical Device regulations.Proficiency in Microsoft Word, Excel, Access, and PowerPoint.Outstanding human relations skills and ability to function in a team environment.Oncology experience preferred.Work Environment

Join a team striving to be a leader in scientific discovery, patient care, and education to improve cancer outcomes. Engage in innovative research and patient-centered care that enhances our understanding of cancer and develops new prevention and treatment strategies. Work in a collaborative environment focused on scientific advancement and patient well-being.

Job Type & Location

This is a Contract position based out of New Brunswick, NJ.

Pay and Benefits

The pay range for this position is $33.00 - $33.00/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 Feb 13, 2026.

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 actalentaccommodation@actalentservices.com for other accommodation options.