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Clinical Research Coordinator
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Sierra Eye Associates
Reno, NV (In Person)
$52,000 Salary, Full-Time
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Job Description
Job Overview We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the coordination and management of clinical trials, ensuring that studies are conducted efficiently, ethically, and in compliance with regulatory standards. Your enthusiasm for advancing medical knowledge and improving patient outcomes will drive your success as you facilitate communication between investigators, participants, and regulatory bodies. This paid position offers an exciting opportunity to contribute to groundbreaking research initiatives that have the potential to transform healthcare. Responsibilities Coordinate all aspects of clinical trial activities, including participant recruitment, enrollment, and follow-up procedures Ensure adherence to study protocols, regulatory requirements, and institutional policies throughout the research process Collect, organize, and maintain accurate study data in accordance with Good Clinical Practice (GCP) guidelines Obtain informed consent from participants by explaining study procedures, risks, and benefits clearly and thoroughly Schedule and conduct study visits, monitor participant safety, and document adverse events promptly Collaborate with investigators, sponsors, and regulatory agencies to facilitate audits and inspections as needed Manage study documentation such as case report forms (CRFs), consent forms, and regulatory submissions with meticulous attention to detail Skills Strong understanding of clinical research processes, regulations (such as FDA or ICH guidelines), and ethical standards Excellent organizational skills with the ability to multitask effectively in a fast-paced environment Exceptional communication skills for engaging with diverse stakeholders including participants, healthcare providers, and regulatory personnel Proficiency in electronic data capture systems and Microsoft Office Suite for documentation purposes Ability to handle sensitive information discreetly while maintaining confidentiality at all times Problem-solving mindset with a proactive approach to addressing challenges during study conduct Prior experience in clinical research coordination or related healthcare roles is preferred but not required; relevant certifications such as CCRP (Certified Clinical Research Professional) are a plus Join us in advancing innovative healthcare solutions! This position is designed for motivated individuals eager to make a meaningful impact through meticulous coordination and compassionate engagement. We value your dedication to excellence in clinical research and look forward to welcoming you to our collaborative team.