Derya Bekar

I am a highly motivated individual with a strong background in Clinical Research, involved in the planning and execution of Phase I clinical trials from the start up to close out phases, ensuring adherence to protocols, timelines and UK regulatory guidelines.

BDD Pharma Ltd from Mary 2021 - Present.

I am responsible for the smooth running of on-site clinical trial activities in accordance with GCP/ICH guidelines and other applicable requirements.

• Preparation and reviewing of study documents
• Maintain accurate and up to date trial documentation, including CRFs, investigator site files (TMF) and electronic trial master files.
• Patient recruitment/building rapport
• Perform accurate collection, review, and reconciliation of clinical trial data using EDC system/Medidata rave.
• Support on site monitoring activities that include reviewing source documents, data entry and aid resolving data queries.
• Assist in tracking and reporting AE/SAEs
• Collaborate with all teams including clinical and medical affairs to ensure seamless communication and execution of trial activities.
• Performing clinical study data analysis.
• Hold weekly clinical meetings

Within BDD Pharma I also have the responsibility of dispensing and authorisation to administer Radiopharmaceutical products to patients taking part in a clinical trial.

Additional Certifications

• GCP
• EDC Castor System
• First Aid
• BLS

Highest education - B.Sc Pharmacology

Graduated 2019 from Glasgow Caledonian University