Stepan Tadevosyan Email & Phone Number

United States

Armenia

Driving data standardization for Medidata's (a Dassault Systèmes Company) Next-Gen solutions.• Responsible for contributing to overall project objectives and specific team deliverables to maintain constant development.• Assign team people to projects and supervise the workflow.• Create/augment specific clinical-trial data master lists to enable analysis.• Analyze aspects of clinical-trial data written in 20 different languages, extract and standardize key study information… Show more Driving data standardization for Medidata's (a Dassault Systèmes Company) Next-Gen solutions.• Responsible for contributing to overall project objectives and specific team deliverables to maintain constant development.• Assign team people to projects and supervise the workflow.• Create/augment specific clinical-trial data master lists to enable analysis.• Analyze aspects of clinical-trial data written in 20 different languages, extract and standardize key study information according to pre-defined and client specific standard conventions.• Make informed decisions based on an in-depth understanding of data type and data management rules and conventions.• Design and implement processes, guidelines, business definitions, metrics and standards for managing information.• Evaluate, manage and resolve issues and risks to ensure business alignment.• Identify areas for modification, develop and test solutions to optimize the workflow.• Lead the process of gathering user and functional requirements for the application that supports data curation workflow.• Regular interactions internal/external.• Managing multiple workstreams and directly coordinating work of 15 people.• Coaching and mentorship.• Recruitment. Show less

Armenia

• Build SAS datasets from clinical database.• Utilize SDTM guidelines to build datasets.• Develop clinical trial data specifications, including CRF annotation, edit rules/checks, query logic and data validations.• Develop test scripts and execution logs for User Acceptance Testing (UAT).• Perform database lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock.• Participate in the review of clinical research documents… Show more • Build SAS datasets from clinical database.• Utilize SDTM guidelines to build datasets.• Develop clinical trial data specifications, including CRF annotation, edit rules/checks, query logic and data validations.• Develop test scripts and execution logs for User Acceptance Testing (UAT).• Perform database lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock.• Participate in the review of clinical research documents (eg. Protocols, Case Report Forms).• Perform training on study trials and create user guides.• Perform comprehensive quality control procedures.• Administer network and data security, including directory, group policy, firewalls, antivirus, etc.• Successfully implemented “OpenClinica” EDC on the local server and take over responsibility for its maintenance as well as data management. Show less

Armenia

• Perform database setup and validation for clinical trials. • Perform database administration including account setup, account maintenance and database lock. • Perform comprehensive quality control procedures.• Understand and comply with core operating procedures and working instructions.• Other DM tasks as deemed appropriate by senior members.

Master Of Engineering - Meng, Food Science And Technology, A+

Bachelor Of Engineering - Be, Food Science And Technology, A+