Senior Data Analyst

4 days ago

Pune Chennai Hyderabad Secunderabad Telangana, India beBeeProgramming Full time
Lead Programmer Role Overview

We are seeking a highly experienced programmer to join our biopharmaceutical organization. This role involves leveraging SAS and other software to develop custom programming code, manage multiple projects, and act as a technical leader for a team of programmers.

  • Develop custom programming code in SAS or other required software to generate summary tables, data listings, graphs, and derived datasets.
  • Ensure outputs meet quality standards and project requirements.
  • Perform validation programming and collaborate with project teams to resolve discrepancies.
  • Manage scheduling and time constraints across multiple projects, setting goals and adapting to changes in priorities.
  • Develop specifications for datasets and outputs of any complexity.
  • Act as the lead programmer, directing the activities of other programming personnel and monitoring their progress.
  • Review project documentation, such as the Statistical Analysis Plan, mock shells, and programming specifications, providing feedback to reduce inefficiencies.
  • Participate in sponsor meetings, kickoff meetings, and bid defense meetings as the programming representative.
  • Contribute to the mentoring of programming personnel by developing training courses and providing guidance to new associates.
  • Serve as a technical expert resource for complex programming questions, with a good working knowledge of clinical drug development, industry standards, and electronic submission requirements.
  • Contribute technical expertise to the development of programming tools and macros for standardization and efficiency.
Required Skills and Qualifications
  • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
  • Knowledge and experience in the use of CDISC Standards for regulatory agency requirements.
  • Experience with submissions to a regulatory agency is preferred.
  • Experience in mentoring others in clinical trial processes and CDISC Standards.
  • Excellent written and verbal communication skills.
  • Ability to manage concurrent programming deliverables and negotiate timelines.
  • Experience with applicable SOPs, WIs, and relevant regulatory guidelines (e.g., ICH).
  • Strong ability to maintain organized, complete, and up-to-date project documentation.

As a leading biopharmaceutical organization, we offer a dynamic and supportive work environment that fosters growth and collaboration. We encourage innovation and creativity, and our team members enjoy a range of benefits, including flexible work arrangements, professional development opportunities, and competitive compensation and rewards.

Our team works together to deliver high-quality solutions that meet the needs of our clients. If you are a motivated and experienced programmer looking for a new challenge, please consider joining our team.

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