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.
Clinical Database Programmer I / II
Job ID R0000034533 , IndiaSummary:
The Clinical Database Programmer is responsible for the programming of high-quality clinical databases. Responsible for supporting assigned segments of the client’s portfolio. Accountabilities to include the design, development, and maintenance of clinical databases, ensuring the integrity of clinical data, application of standards supporting consistency in asset/submission data.
Responsibilities:
Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans.
Complies with applicable SOPs and work practices.
Learn client’s database technologies.
Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data.
Qualifications:
Bachelor's degree in Life Science, Computer Science or equivalent.
Minimum of 1+ years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions.
Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills.
Technical skills and experience using relational databases (e.g. Oracle InForm, Oracle DMW, MS SQL Server or MS Access).
Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills.
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).
Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.).
Understanding regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable.
#LI-REMOTE
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs