Clinical Research Coordinator

Duties Oversee and coordinate clinical research studies in accordance with GCP and FDA regulations Manage data collection, entry, and analysis processes Supervise research staff involved in the studies Ensure compliance with protocols, regulatory requirements, and ethical standards Conduct clinical laboratory procedures as needed Review and maintain documentation for accuracy and completeness Collaborate with investigators and healthcare professionals to facilitate research activities Qualifications Bachelor's degree in a related field such as healthcare or life sciences Proficiency in medical terminology and clinical research practices Experience in supervising staff and managing clinical research projects Knowledge of compliance management and FDA regulations Experience in FDA approved clinical trials (2+ years preferred) Strong skills in data management and documentation review Blood Draw experience (preferred) Job Type: Full-time Pay: $23.71 - $25.85 per hour Benefits Flexible schedule Schedule 8 hour shift Monday to Friday Ability to Relocate Bloomfield Hills, MI 48302: Relocate before starting work (Required) Work Location: In person #J-18808-Ljbffr The Voluntary Protection Programs Participants' Association, Inc