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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Statistical Programmer I (Russia - Moscow or St. Petersburg)Job ID 66984BR St Petersburg, St.-Petersburg, Russia
The Statistical Programmer I works with close supervision to support various programming activities related to the analysis and reporting of clinical study data. General areas of responsibility also include: import/export programming specification development, test data creation and test data entry, import/export programming functional testing, as well as mapping specifications to support relevant data standards.
Deliver best value and high quality service.
Check own work in an ongoing way to ensure first-time quality.
Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to ensure traceability and regulatory compliance.
Ensure compliance with WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and participate in internal/external audits and regulatory inspections as required.
Use efficient programming techniques to produce low-medium complexity derived datasets, tables, figures and data listings.
Create, implement and execute import and export programs, in either standard format, client specific format or CDISC compliant format depending on nature of request.
Develop mapping specification for data exports in accordance with applicable standards.
QualificationsMinimum Work Experience
Relevant work experience recommended preferably in clinical research industry and experience in SAS or other programming languages preferred.
Experience in SAS.
Knowledge of the programming and reporting process within the Statistical Programming Department.
Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
Demonstrate ability to learn new systems and function in an evolving technical environment.
Attention to detail.
Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently.
Work effectively in a quality-focused environment.
Effective time management in order to meet daily metrics or team objectives.
Show commitment to and perform consistently high quality work.
First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience.
Competent in written English.
Good communication skills.
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