Clinical Research Assistant (FOCD-Research)

The Clinical Research Assistant will support the research team in conducting clinical trials, working under the direct supervision of the Principal Investigator, Site Manager and Study Coordinator. He/ She will play a key role in the daily operations of research studies, ensuring protocols are followed and assisting with participant management.

Requirements

• Screening potential participants by phone and assessing their interest in study involvement.
• Assisting with participant visit management, including administrative support during visits.
• Scheduling participants for upcoming visits, ensuring all protocol requirements are met.
• Sending reminders via call or text regarding upcoming visits and providing any specific instructions (e.g., fasting, bringing medication bottles, etc.).
• Preparing for study visits by organizing materials and ensuring compliance with the study protocol.
• Managing both physical and electronic study documents, ensuring accurate filing and organization.
• Entering data from study visits into clinical trial management systems (CTMS) and secure electronic databases (EDC) as authorized.
• Performing study visit procedures as delegated by the Investigator including but not limited to vital signs, ECG, Phlebotomy, lab processing.
• Promoting a team-oriented work environment, prioritizing safety and mutual respect among colleagues.
• Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services.