The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations. This position may direct the work of junior staff, train personnel and direct the work of a Clinical Research Assistant as assigned.
Additionally, this position may involve supervising junior staff, providing training to personnel, and overseeing the activities of a Clinical Research Assistant as required. Preference will be given to individuals with a background/degree in bioengineering and device work.
Work Schedule: Monday-Sunday 9am-5pm