Anna Nadiryan

• Study and site management and monitoring of clinical trials
• Coordinate and schedule protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
• Collaborate with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
• Submit routine monitoring reports and follow-up letters to facilitate internal and external communication.
• Monitor safety of human subjects and oversew consent procedures to comply with local and federal regulations.
• Conduct meetings with sponsor representatives to discuss clinical study developments.
• Review data queries and listings and worked with study centers to resolve data discrepancies.

• Replicate flow, style, and overall meaning of original texts.
• Apply cultural understanding to discern specific meanings beyond literal written words.
• Review final works to spot and correct errors in punctuation, grammar, and translation.
• Translate documents from Russian to English and vice versa.

• Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
• Conducted meetings with sponsor representatives to discuss clinical study developments.
• Implemented electronic data capturing systems to adhere with clinical research guidelines.
• Reviewed data queries and listings and worked with study centers to resolve data discrepancies.

Developed pharmacovigilance procedures pack.

• Managed routine safety information;
• Submitted periodic and expedited reports to Regulatory Authority;
• Trained AZ Russia personnel in pharmacovigilance responsibilities
• Tutored the PSM deputy
• Provided support to AZ Russia personnel regarding corporate policies and processes
• Developed improved pharmacovigilance procedures.

• Managed adverse event information;
• Submitted expedited safety reports to company's global pharmacovigilance unit;
• Collaborated with regulatory authorities;
• Delivered trainings on pharmacovigilance to affiliate personnel, developed and mainlined the local SOP.

• Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
• Conducted meetings with sponsor representatives to discuss clinical study developments.
• Implemented electronic data capturing systems to adhere with clinical research guidelines.
• Reviewed data queries and listings and worked with study centers to resolve data discrepancies.

• Senior editor of press review bulletins of Russian mass media, supervisor

• Participation in clinical research projects;
• Engineering of analytical instruments and structuring of obtained data (MS Excel, OriginPro).

• Molecular and cell biology)
• Participation in fundamental scientific research projects;
• Statistical analysis of experimental data (MS Excel);
• Co-authorship in publications in scientific periodicals., Participation in fundamental scientific research projects;
• Statistical analysis of experimental data (MS Excel);
• The results of the research were presented as a term paper
• Execution of clinical assays (semen analysis)

• Performed routine laboratory tests at the Laboratory of genetic malfunctions of spermatogenesis
• Prepared term thesis.