-Prepare study-specific Clinical Trial Agreements based on the requirements of study sponsors. -Negotiate the contract language with the appropriate party at the sites.-Finalize all required contract-related documents and/or amendments.-Prepare, negotiate, analyze, escalate and finalize agreements for external vendor services (Site -Management Organizations agreements, radiology agreements etc.)-Work simultaneously on numerous contracts and maintain status tracking tool for… Show more -Prepare study-specific Clinical Trial Agreements based on the requirements of study sponsors. -Negotiate the contract language with the appropriate party at the sites.-Finalize all required contract-related documents and/or amendments.-Prepare, negotiate, analyze, escalate and finalize agreements for external vendor services (Site -Management Organizations agreements, radiology agreements etc.)-Work simultaneously on numerous contracts and maintain status tracking tool for individual sites for each study.-Maintain communication and participate in regular meetings with Site Activation Leads Show less

- Performed the raw material analysis according to USP/EP monographs or the in-house methods.- Performed the analytical method evaluation, method development and method validation(Linearity, Recovery, Specificity, LOQ-LOD, Forced degradation, Precision etc.) in accordance with ICH guidelines.- Performed the finished product and stability sample testing such as assay, degradation products, content uniformity, residual solvents, dissolution and water determination.- Implement the… Show more - Performed the raw material analysis according to USP/EP monographs or the in-house methods.- Performed the analytical method evaluation, method development and method validation(Linearity, Recovery, Specificity, LOQ-LOD, Forced degradation, Precision etc.) in accordance with ICH guidelines.- Performed the finished product and stability sample testing such as assay, degradation products, content uniformity, residual solvents, dissolution and water determination.- Implement the method transfer of the raw material, finished product, cleaning agent and cleaning validation of current product from the related pharmaceutical equipment.- Experienced in writing method validation protocol/report, method transfer protocol/report and analytical instrument’s SOPs.- Maintain accurate, well-kept laboratory notebook. Show less

Participated in the project of the synthesis of thermally activated delayed fluorescence small molecules for active-matrix OLED devices in Prof. Dr. Levent Toppare Organic Synthesis Laboratory in Polymeric Materials.

Gained basic knowledge of the analytical method validation parameters, dissolution testing and drug production.