Jobs at Parexel
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 II
Job ID 84354BR , RemoteResponsibilities:
- Act as an internal Subject Matter Expert and Work independently to support various programming activities related to analysis and reporting of clinical study data.
- Perform as Statistical Programming Coordinator on projects and interact with Sponsors, Data Operation Lead and other functions as a key contact with regard to statisticalprogramming issue.
- Use efficient programming techniques to produce and QC of derived datasets and TLF.
- Create/modify standard macros and applications to improve the efficiency.
- Develop wider knowledge of SAS and other relevant programming languages and processes.
- Understanding regulatory requirements concerning industry technical standards, maintain all supporting documentation in accordance with WSOPs/guidelines.
- Provide relevant training and mentorship to staff and project teams A graduate or master degree in a relevant educational filed life science, computer, pharmacy, others.
- Proficiency in SAS and knowledge of programming and reporting process. Excellent experience with TLF, SAS coding, Macros, SQL, PROC reports, SDTM, ADAM(preferred)
Requirements:
- Knowledge of WSOPs/ICH-GCP and System Life Cycle methodologies.
- Excellent communication (written & oral) skills and strong leadership ability.
- Strong organizational skills, flexible to change and team work.
- Ability to manage complex projects and business operational skills Study lead experience.
- For Associate Manager and Manager Role you must have people management (LM)experience.
- First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent
- Competent in written English.
- Good communication skills.
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