Position Summary:
The Instructor supports the planning, coordination, and execution of clinical trials. This role involves ensuring that trials are conducted according to regulatory requirements, study protocols, and Good Clinical Practice (GCP) standards, while providing administrative and operational support to the clinical team.

Key Responsibilities:


+ Assist in the management and coordination of clinical trials, including participant recruitment and enrollment.

+ Maintain accurate trial documentation, including case report forms, regulatory binders, and study databases.

+ Support monitoring activities and prepare study materials for site visits and audits.

+ Communicate with study sites, investigators, and vendors to facilitate smooth trial operations.

+ Assist with data collection, entry, and quality checks to ensure data integrity.

+ Ensure compliance with institutional policies, FDA regulations, and GCP guidelines.<...