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