Clinical Research Coordinator
📋 Role Overview & Responsibilities
Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women's health!
HighlightsPlay a major role in advancing medicine with a team dedicated to the patient experience!Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays)Competitive Base Salary Gain experience in the fast-growing world of clinical research and develop skills that are in high demandMonday - Friday 8:30 AM - 5 PM with some flexibility to meet patient schedulesThe company is invested in growth, providing employees with unique opportunities for career advancementJoin a dedicated team at a large site with opportunities for advancement at the site and site network level.
PositionThe Clinical Research Coordinator (CRC) is central to conducting and managing clinical trials, tasked with obtaining informed consent, executing study protocols, handling human specimens, and ensuring meticulous documentation and communication. This role demands a blend of precision, organization, and professional integrity, underscored by a deep commitment to providing an exceptional patient experience throughout the research journey. By fostering clear communication, demonstrating empathy, and ensuring participants feel respected and valued, CRCs play a vital role in enhancing participant engagement and adherence to study protocols.
CompanyOur client is a Clinical Research site network with over 17 research sites across the United States. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, women's health, and vaccines. They are a fast-growing site network with plans to grow from 17 sites to over 30 sites in 2024 alone.
QualificationsBachelor's degree preferred, but not requiredPhlebotomy experience is required, EKG or other patient labs/processes preferredPreferably 2+ years of experience as a Clinical Research CoordinatorFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office Suite
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This position is located in San Antonio, TX with potential relocation and sponsorship assistance depending on candidate qualifications.
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