Impactful Oncology Clinical Trials Coordinator

Regional Cancer Care Associates; Howell Township (NJ); On-site; USD 77,366,000 - 104,698,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Wellness program

Health savings account

Flexible spending accounts

401(k) retirement plan

Life insurance

Short-term disability insurance

Long-term disability insurance

Employee Assistance Program (EAP)

Paid Time Off (PTO) and holiday pay

Tuition discounts

Job summary

Regional Cancer Care Associates in Howell, NJ seeks a Research Coordinator to oversee each assigned clinical trial from start to finish under Clinical Trial Management guidance.

Ideal candidate has oncology interventional trial experience, CCRP/CCRP/SOCRA certification, and strong multitasking and communication skills. Full-time role with comprehensive benefits and on-site work. Oncologic research focus and patient-centered care are central.

Qualifications

• Minimum 1 year of oncology interventional clinical trials.
• Certified Clinical Research Professional (ACRP/SoCRA) required.
• High school diploma with oncology trial experience.
• Able to travel onsite Monday to Friday 9 am to 5 pm.
• Strong communication and regulatory experience is a plus.

Responsibilities

• Oversee assigned clinical trials from start to finish.
• Screen and recruit patients using EMR, EDC, CTMS.
• Maintain enrollment logs and schedule visits.
• Enter data within 24 hours and resolve data queries within 5 days.
• Ensure regulatory documents and HIPAA/FDA compliance.

Skills

Oncology clinical trials

Regulatory knowledge

Interpersonal communication

Time management

Education

High School diploma with oncology trial experience

ACRP/SoCRA CCRP certification

Tools

EMR systems

EDC

CTMS

Job description

Regional Cancer Care Associates in Howell, NJ seeks a Research Coordinator to oversee each assigned clinical trial from start to finish under Clinical Trial Management guidance.

Ideal candidate has oncology interventional trial experience, CCRP/CCRP/SOCRA certification, and strong multitasking and communication skills. Full-time role with comprehensive benefits and on-site work. Oncologic research focus and patient-centered care are central.