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Clinical Research Coordinator
2 months ago
Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women's health
Highlights
- Play 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 demand
- Monday - Friday 8:30 AM - 5 PM with some flexibility to meet patient schedules
- The company is invested in growth, providing employees with unique opportunities for career advancement
- Join a dedicated team at a large site with opportunities for advancement at the site and site network level.
Position
The 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.
Company
Our 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.
Qualifications
- Bachelor's degree preferred, but not required
- Phlebotomy experience is required, EKG or other patient labs/processes preferred
- Preferably 2+ years of experience as a Clinical Research Coordinator
- Familiar with e-source reporting via an electronic platform
- A clear understanding of ICH, FDA, and GCP regulations
- Impeccable organizational skills and attention to detail
- Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
- An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
- High-level critical thinking skills
- Working knowledge of medical terminology and lab collection/processing/storage procedures
- Proficiency with computers and Microsoft Office Suite
