Oncology Clinical Research Program Manager — Lead Trials

Vitalief; United States; On-site; USD 115,000 - 145,000; Full time

Benefits offered by this job

20 PTO days

9 paid holidays

Life insurance

Disability coverage

401(k) retirement plan

Healthcare benefits

Job summary

Vitalief seeks a Clinical Research Program Manager to oversee Phase II–IV oncology trials at a premier research center in Somerset, NJ. You will lead operations across two sites, ensuring protocol execution, enrollment, data collection, and regulatory compliance (GCP, FDA, HIPAA, IRB).

The ideal candidate has 3+ years in oncology clinical research with supervisory experience; RN preferred. The role is on-site four days weekly in Somerset and one day in Hamilton, with standard hours Monday–Friday.

Qualifications

• Bachelor’s degree in Nursing or related field required; RN preferred.
• 3+ years oncology clinical research experience and managing trials.
• 1–2 years of supervisory or management experience.

Responsibilities

• Lead daily oncology clinical research operations across two locations.
• Oversee protocol implementation, study activation, enrollment, data collection.
• Mentor and develop a small clinical research team.

Skills

Leadership

Communication

Time management

Mentoring

Project management

Education

Bachelor's degree in Nursing, Health Sciences, Life Sciences, Public Health, or related field

Master's degree preferred

Tools

CTMS

EDC platforms

OnCore

Microsoft Office

Job description

Vitalief seeks a Clinical Research Program Manager to oversee Phase II–IV oncology trials at a premier research center in Somerset, NJ. You will lead operations across two sites, ensuring protocol execution, enrollment, data collection, and regulatory compliance (GCP, FDA, HIPAA, IRB).

The ideal candidate has 3+ years in oncology clinical research with supervisory experience; RN preferred. The role is on-site four days weekly in Somerset and one day in Hamilton, with standard hours Monday–Friday.