Clinical Database Programmer I (Delhi)

Summary: 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 clients 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). - Robust 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 .