Bassey Etuk

• Conduct site initiation visit and reports
• Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
• Implemented electronic data capturing systems to adhere with clinical research guidelines.
• Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
• Provided clinicians with data to conduct clinical trials and determine methods to prevent, screen for, diagnose and treat disease.
• Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.

Establish monitoring visit frequency and communicate to site

Review Protocols requirements

Ensure all adverse effects are reported according to regulations and company policy

visit sites as scheduled required

Review protocol compliance, focusing on inclusion and exclusion

Prepare final study report

Ability to visit multiple site independently and as a team