We are seeking a dedicated Clinical Research Assistant and Coordinator to join our team. The individual will be responsible for managing and coordinating clinical trials and research studies in compliance with regulatory guidelines and protocols. This role involves working closely with principal investigators, research staff, and study participants to ensure the smooth operation of the clinical research process.

Key Responsibilities:

• Coordinate and oversee all aspects of clinical trials, including participant recruitment, enrollment, and follow-up.
• Assist in the development of study protocols, consent forms, and data collection tools.
• Ensure all research activities comply with ethical standards, institutional policies, and regulatory requirements (FDA, GCP, IRB).
• Collect, manage, and analyze clinical data; maintain accurate and organized records.
• Communicate with study sponsors, monitor study progress, and resolve any issues that arise.
• Schedule and conduct participant visits, ensuring compliance with study protocols.
• Assist with the preparation of regulatory documents and reports.
• Maintain confidentiality and protect the integrity of participant data.