Clinical Research Coordinator

Job Summary We are seeking a dynamic and detail-oriented Clinical Research Coordinator to join our innovative research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and study protocols. Your enthusiasm for advancing medical knowledge will drive the successful completion of research projects that impact patient care worldwide. This paid position offers an exciting opportunity to develop your expertise in clinical development while supporting groundbreaking health initiatives. Duties Coordinate and monitor all aspects of clinical trials, including participant recruitment, enrollment, and follow-up procedures Review and verify study documentation, ensuring accuracy and adherence to regulatory guidelines such as FDA regulations and ICH GCP standards Conduct patient monitoring by collecting vital signs, blood samples through phlebotomy, and recording clinical data accurately in electronic medical records (EMR) systems Supervise research staff and collaborate with multidisciplinary teams to ensure smooth trial operations Manage data collection, entry, and management using statistical software and adhere to CDISC standards for data consistency Ensure compliance with HIPAA regulations to protect patient privacy and confidentiality Prepare reports, maintain detailed documentation review logs, and assist in regulatory submissions for trial approval Skills Proven supervising experience in clinical research settings with the ability to lead teams effectively Extensive knowledge of clinical trials management, including protocol development and regulatory compliance Strong understanding of medical terminology, clinical laboratory procedures, and blood sampling techniques Proficiency in data management tools, statistical software, and EMR systems used in clinical research environments Familiarity with FDA regulations, ICH GCP guidelines, and HIPAA privacy standards to ensure trial integrity and participant safety Experience with clinical development processes from early-phase studies to late-stage trials Certification in Good Clinical Practice (GCP) from a recognized issuer such as CA or equivalent is highly desirable Excellent analysis skills for interpreting clinical data and identifying trends or discrepancies Ability to review complex documentation thoroughly while maintaining attention to detail Knowledge of CDISC standards for data collection and reporting within clinical trials Join our team to contribute meaningfully to medical advancements while advancing your career in a fast-paced, rewarding environment. We are committed to fostering a culture of excellence where your skills make a tangible difference in patient outcomes worldwide.

Pay:

$20.00 - $25.00 per hour

Benefits:

401(k) Dental insurance Health insurance Paid time off

Work Location:

In person