Clinical Research Coordinator
Virtual US
About Cleerly
Weâre Cleerly â a healthcare company thatâs revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the worldâs leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which will enable rapid growth and continued support of our mission. Our teams work remotely and have access to our offices in Colorado, New York, and Portugal.Â
Cleerly is creating a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerlyâs solutions are supported by more than a decade of performing some of the worldâs largest clinical trials to identify important findings beyond symptoms that increase a personâs risk of heart attacks.Â
At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description.Â
About the Opportunity
We are seeking a detail-oriented and motivated Clinical Research Coordinator to join our team. The ideal candidate will have at least 1 year of experience in clinical research and possess a solid understanding of trial operations. In this role, you will be responsible for coordinating all aspects of clinical trials, from patient recruitment and data collection to regulatory compliance. This is an excellent opportunity to gain hands-on experience and contribute to cutting-edge clinical studies in a dynamic and supportive environment.
Responsibilities
- Coordinate the day-to-day operations of clinical trials, ensuring compliance
- with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Assist in the identification, recruitment, and screening of potential study participants in accordance with study protocols.
- Obtain informed consent from study participants and ensure their ongoing compliance with study procedures.
- Collect, manage, and enter study data accurately into electronic data capture systems, ensuring data integrity and adherence to timelines.
- Prepare and maintain study-related documentation, including case report forms, source documents, and regulatory binders.
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Benefits/PerksDynamic environment Hands-on experience Medical, Dental, and Vision plans Parental leave benefits Remote-first company Remote work Stock options
Tasks- Coordinate clinical trials
- Ensure regulatory compliance
- Prepare documentation
AI Clinical Research Clinical trials Communication Compliance Confluence Data Collection Data Management Docs Drive FDA regulations GCP Gmail Google Workspace Healthcare Jira Marketing Organizational R Regulatory Compliance Sales Sheets Slack Slides Zoom
Experience1 years
EducationBachelor's degree Biology Engineering Health Related Field Nursing Public health Related Field
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