Hybrid Clinical Research Coordinator - Cardio Registry

Vitalief Inc.; Newark (NJ); Hybrid; USD 65,000 - 78,000; Full time

Benefits offered by this job

20 PTO days

9 paid holidays

Company-paid life insurance

Short- and long-term disability

401(k) retirement plan

Robust healthcare options

Job summary

Vitalief Inc. is looking for a Clinical Research Coordinator (CRC) to support a vascular medical device registry study in Newark, NJ. The ideal candidate has at least 2 years of CRC experience, a strong interest in cardiovascular research, and is able to work independently. The role offers a hybrid work setup with 2-3 days onsite and a salary range between $65,000 and $78,000 based on experience.

The role includes managing study activities, ensuring compliance, and collaborating with the research team. Ideal candidates must hold a relevant Bachelor's degree and have experience in clinical research.

Qualifications

• Minimum 2 years of clinical research coordination experience.
• Experience with regulatory documentation and IRB submissions.
• Strong organizational skills to manage multiple responsibilities.

Responsibilities

• Manage day-to-day study activities as the primary site coordinator.
• Identify, enroll, and maintain follow-up with study participants.
• Ensure compliance with protocol and research standards.

Skills

Clinical research coordination

Attention to detail

Project management

Communication

Regulatory documentation

Education

Bachelor's degree in health science, life science, nursing, or related field

Tools

EPIC

Microsoft Office

CTMS systems

Job description

Vitalief Inc. is looking for a Clinical Research Coordinator (CRC) to support a vascular medical device registry study in Newark, NJ. The ideal candidate has at least 2 years of CRC experience, a strong interest in cardiovascular research, and is able to work independently. The role offers a hybrid work setup with 2-3 days onsite and a salary range between $65,000 and $78,000 based on experience.

The role includes managing study activities, ensuring compliance, and collaborating with the research team. Ideal candidates must hold a relevant Bachelor's degree and have experience in clinical research.