Clinical Research Coordinator

Responsibilities

• Affords assistance in the implementation and coordination of research studies and projects.
• Assumes responsibility for study-specific duties under the guidance of the Principal Investigator (PI).
• Collaborates with the PI and supervisor to organize, plan, and execute research efficiently and promptly.
• Participates in feasibility studies, resource allocation, and study planning activities, including conducting internal training sessions to implement protocols and prevent deviations.
• Engages in recruitment strategies for potential participants and oversees the enrollment process for clinical trials as directed by the PI.
• Ensures adherence to study parameters before and during research participant visits and assessments.
• Extracts and records physical findings, laboratory data, and other pertinent details onto required data collection forms accurately and within stipulated timeframes.
• Attends investigator meetings, pre-study site visits, and other study-related visits by monitors or sponsors, and participates in in-house protocol meetings.
• Facilitates the informed consent process with the Investigator to ensure participants and their families (if applicable) comprehend the consent form and understand their responsibilities in the study.
• Provides participant instructions and serves as the primary point of contact for study-specific inquiries, concerns, or events.
• Accurately records and extracts data from source documentation onto required forms (paper or electronic) in a timely manner.
• Maintains accurate and timely source documentation and prepares study documents for archiving according to timelines.
• Displays comprehensive knowledge of protocol requirements and Good Clinical Practice (GCP) guidelines.
• Performs other related duties as assigned or required.

Qualifications

• Bachelor's Degree (Required)