Senior Oncology CRC — Lead Interventional Trials | Hybrid

Vitalief; Newark (NJ); Hybrid; USD 75,000 - 85,000; Full time

Benefits offered by this job

20 PTO days

401(k) retirement plan

Comprehensive healthcare benefits

Job summary

Vitalief is looking for a Senior Clinical Research Coordinator to manage a portfolio of oncology clinical trials in Newark, NJ. The role is full-time and requires at least 3 years of relevant experience to oversee multiple studies, ensuring compliance with protocols and regulations.

Candidates should have a Bachelor’s degree in a related field and experience in clinical trial execution. The position provides competitive salary and benefits including paid time off and a hybrid work schedule after the initial training period.

Qualifications

• Minimum of 3 years of clinical research coordination experience.
• Required oncology clinical trial experience.
• Ability to manage multiple concurrent studies.

Responsibilities

• Support execution of Phase II–IV oncology clinical trials.
• Manage a portfolio of 15–20 active clinical trials.
• Ensure compliance with study protocols and regulatory requirements.

Skills

Oncology clinical trial experience

Patient identification and enrollment

Regulatory compliance

Mentoring junior CRCs

Proficiency with EPIC and OnCore™ CTMS

Strong communication skills

Education

Bachelor’s degree in health science or a related field

Tools

Microsoft Office applications

Clinical research systems

Job description

Vitalief is looking for a Senior Clinical Research Coordinator to manage a portfolio of oncology clinical trials in Newark, NJ. The role is full-time and requires at least 3 years of relevant experience to oversee multiple studies, ensuring compliance with protocols and regulations.

Candidates should have a Bachelor’s degree in a related field and experience in clinical trial execution. The position provides competitive salary and benefits including paid time off and a hybrid work schedule after the initial training period.