Clinical Research Coordinator

About the Role

This is a full-time, on-site position responsible for managing the daily operations of clinical trials while ensuring strict compliance with study protocols, regulatory requirements, and ethical standards.

You will play a key role in maintaining study integrity, protecting patient safety, and ensuring data accuracy.

Key Responsibilities

• Obtain and properly document informed consent
• Ensure protocol adherence and regulatory compliance
• Maintain accurate and organized study documentation
• Coordinate participant recruitment and retention
• Collect and manage study data
• Work closely with investigators, sponsors, and site staff
• Ensure timelines and milestones are met

Qualifications

• Minimum 2 years of experience

Strong experience with Informed Consent processes

• Solid understanding of clinical study protocols
• Prior experience in clinical research, preferably in a regulated environment
• Strong focus on patient safety, compliance, and data accuracy
• Excellent organizational and communication skills
• Ability to work independently and collaboratively
• Bachelor’s degree in a healthcare-related field or relevant certification preferred

Why Join Omnicure?

At Omnicure, we are more than a research site we are driven by purpose. You will be part of a team committed to integrity, innovation, and improving patient outcomes through high-quality clinical research.

If you are passionate about advancing medicine and making a meaningful impact, we would love to hear from you.

• Apply now or message us directly to learn more. ssuarez@omnicureresearch.com

Job Type: Full-time

Pay: $22.00 - $27.00 per hour

Work Location: In person