Senior Clinical Research Coordinator

Job Overview
We are seeking a highly motivated and experienced Senior Clinical Research Coordinator to lead and oversee complex clinical trials within our research team. This pivotal role involves managing all aspects of clinical study execution, ensuring compliance with regulatory standards, and maintaining meticulous documentation. The ideal candidate will possess strong supervisory skills, extensive knowledge of clinical trials management, and a passion for advancing medical research. Join us to contribute to groundbreaking studies that improve patient outcomes and shape the future of healthcare.

Duties

• Lead and supervise clinical research teams, providing guidance and mentorship to ensure smooth trial operations
• Manage the full lifecycle of clinical trials, including planning, initiation, monitoring, and closeout activities
• Review and ensure accuracy of all study documentation in accordance with FDA regulations and ICH GCP standards
• Monitor patient safety by overseeing patient recruitment, informed consent processes, and ongoing patient assessments
• Conduct data collection, entry, and management using EMR systems and statistical software to support data integrity and analysis
• Perform clinical laboratory procedures such as blood sampling, phlebotomy, and vital signs measurement with precision
• Ensure compliance with HIPAA regulations and maintain confidentiality of patient information throughout all trial phases

Skills

• Supervising experience in a clinical research setting with proven leadership capabilities
• Extensive knowledge of clinical trials management, including protocol adherence and regulatory compliance
• Strong understanding of medical terminology, FDA regulations, ICH GCP standards, and CDISC data standards
• Proficiency in clinical data management tools, statistical software, and EMR systems for accurate data collection and analysis
• Experience with clinical laboratory procedures such as blood sampling and blood testing techniques
• Excellent documentation review skills to ensure accuracy and regulatory compliance
• Ability to monitor vital signs accurately while maintaining patient safety and comfort
• Familiarity with clinical development processes, research methodologies, and compliance management practices
• Certification in ICH GCP (Good Clinical Practice) from a recognized issuer such as CA or equivalent is required
• Background in nursing or phlebotomy is preferred to enhance patient monitoring capabilities
• Strong analysis skills to interpret research data effectively while adhering to CDISC standards

Join our team as a Senior Clinical Research Coordinator to make a meaningful impact on health sciences through meticulous research oversight. We value your expertise in managing complex trials while fostering a collaborative environment dedicated to innovation and excellence.

Pay: From $30.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Work Location: In person