Clinical Research Coordinator

Job Summary: We are seeking a highly motivated and organized individual to join our team as a Clinical Research Coordinator.

Key Responsibilities:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.
• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns.
• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
• Plan and coordinate logistical activity for study procedures according to the study protocol.

Requirements:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
• Basic knowledge of medical terminology.
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.
• Good organizational skills with the ability to pay close attention to detail.

About Iqvia: We are a leading healthcare company that provides innovative solutions to improve patient outcomes and healthcare systems.