Clinical Research Nurse

About the role

Oncology Clinical Research Nurses at Actalent are responsible for coordinating oncology clinical trials, supporting patient enrollment and informed consent processes, and ensuring compliance with regulatory requirements.

• Coordinate the start-up and activation of oncology clinical trials, including protocol review, study preparation, and staff education.
• Screen patients for eligibility, review medical records, and support patient enrollment and informed consent processes.
• Coordinate study-related visits, procedures, testing, treatments, and patient follow-up activities.
• Monitor, document, and report adverse events, serious adverse events (SAEs), and protocol deviations in accordance with regulatory requirements.
• Maintain accurate research documentation, source records, case report forms (CRFs), and study files.
• Collaborate with investigators, sponsors, and multidisciplinary teams to support study conduct, audits, monitoring visits, and data query resolution.
• Ensure compliance with Good Clinical Practice (GCP), Food and Drug Administration (FDA), Institutional Review Board (IRB), institutional, state, and federal regulations.
• Educate patients and caregivers on clinical trial participation, treatment plans, and symptom management.
• Carefully coordinate biospecimen collection, processing, and shipment according to study protocols.

Qualifications

• Active RN license in the State of New Jersey (or ability to obtain prior to start)
• Must have 3 years of oncology nursing experience
• Active BLS certification
• Bachelor's Degree in Nursing (BSN)
• Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN)

Responsibilities

• Experience in clinical research is preferred
• Coordinate the start-up and activation of oncology clinical trials, including protocol review, study preparation, and staff education.
• Screen patients for eligibility, review medical records, and support patient enrollment and informed consent processes.
• Coordinate study-related visits, procedures, testing, treatments, and patient follow-up activities.
• Monitor, document, and report adverse events, serious adverse events (SAEs), and protocol deviations in accordance with regulatory requirements.
• Maintain accurate research documentation, source records, case report forms (CRFs), and study files.
• Collaborate with investigators, sponsors, and multidisciplinary teams to support study conduct, audits, monitoring visits, and data query resolution.
• Ensure compliance with Good Clinical Practice (GCP), Food and Drug Administration (FDA), Institutional Review Board (IRB), institutional, state, and federal regulations.
• Educate patients and caregivers on clinical trial participation, treatment plans, and symptom management.
• Carefully coordinate biospecimen collection, processing, and shipment according to study protocols.

Job Type & Location

This is a Contract to Hire position based out of Livingston, NJ.

Pay And Benefits

The pay range for this position is $55.00 - $63.00/hr.

Requirements

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 fully onsite position in Livingston, NJ.

Application Deadline

This position is anticipated to close on Jul 16, 2026.