Senior Clinical Research Coordinator

Job Summary We are seeking a dynamic and experienced Senior Clinical Research Coordinator to lead and manage complex clinical trials with enthusiasm and precision. In this pivotal role, you will oversee the coordination of clinical research activities, ensure compliance with regulatory standards, and facilitate seamless communication among research teams, participants, and stakeholders. Your expertise will drive the successful execution of clinical studies, contributing to groundbreaking medical advancements. This position offers an exciting opportunity to work at the forefront of clinical development within a collaborative and innovative environment. Responsibilities Lead the planning, initiation, and management of clinical trials in accordance with FDA regulations, ICH GCP guidelines, and institutional policies. Supervise and mentor junior research staff, ensuring high-quality data collection, documentation review, and adherence to study protocols. Coordinate patient recruitment, screening, enrollment, and ongoing monitoring to ensure participant safety and protocol compliance. Oversee clinical procedures such as blood sampling, vital signs measurement, phlebotomy, and patient assessments using EMR (Electronic Medical Record) systems. Review and verify clinical trial documentation for accuracy, completeness, and regulatory compliance; prepare reports for regulatory submissions. Manage data collection processes utilizing statistical software and CDISC standards to ensure data integrity for analysis. Ensure all activities comply with HIPAA regulations to protect patient privacy and confidentiality; maintain meticulous records of study activities. Experience Proven supervising experience in a clinical research setting or related healthcare environment. Extensive knowledge of clinical trials management, including patient monitoring, data management, and regulatory compliance. Strong understanding of medical terminology, clinical laboratory procedures, and blood sampling techniques. Experience working with EMR systems and familiarity with FDA regulations and ICH GCP guidelines. Demonstrated ability to review complex documentation accurately while maintaining attention to detail. Proficiency in statistical software used for data analysis in clinical research settings. Certification in ICH GCP (Good Clinical Practice) from a recognized issuer for CA or equivalent certification is required. Background in nursing or phlebotomy is highly desirable; experience with clinical development phases is preferred. Join us as a Senior Clinical Research Coordinator to make a meaningful impact on health innovations! Your expertise will support vital research efforts that improve lives worldwide while advancing your career in a vibrant team dedicated to excellence in clinical science.

Job Type:

Full-time Pay:

$55,904.52 - $67,325.87 per year

Work Location:

In person