Clinical Research Nurse II

Actalent is hiring a Clinical Research Nurse II in South Camden, Camden County, USA. This full‑time role offers a salary of $53,299.91 and requires a New Jersey RN license and prior clinical research experience.

Key Responsibilities

• Prepare and submit IRB protocols, informed consent documents, and regulatory paperwork.
• Identify, screen, and recruit eligible patients for clinical trial participation.
• Coordinate patient visits, collect data, and ensure protocol adherence.
• Maintain accurate source documents and electronic case report forms.
• Collaborate with investigators, study coordinators, and sponsor representatives.
• Monitor safety, report adverse events, and ensure compliance with GCP and FDA regulations.
• Provide patient education, support, and follow‑up throughout the study.

Required Qualifications

• Active RN license in New Jersey.
• Minimum 2 years of clinical nursing experience with documented clinical research exposure.
• Strong knowledge of IRB processes, FDA regulations, and Good Clinical Practice.
• Excellent communication, organizational, and interpersonal skills.
• Proficiency with electronic data capture systems and Microsoft Office.

Preferred Experience

• Experience in oncology, cardiology, or other therapeutic areas.
• Certification as a Clinical Research Professional (CCRP) or equivalent.

Compensation & Benefits

Salary: $53,299.91 annually. Competitive benefits package including health insurance, 401(k) match, paid time off, and professional development support.

Frequently Asked Questions

Do I need a New Jersey RN license for this role?

Yes, an active RN license in New Jersey is mandatory.

What type of clinical research experience is required?

At least two years of nursing experience that includes direct involvement in clinical trial coordination or monitoring.

Is remote work possible for this position?

The role requires on‑site patient interaction at the South Camden facility, so remote work is not offered.