Statistical Programmer

2 days ago

Bengaluru, India George Clinical Full time

We are expanding We are hiring Statistical Programmer-I/II We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.


Who are we?

  • A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence.
  • 20+ years of experience, 500+people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe.
  • Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration, and post-marketing trial.
  • We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, and cardiovascular and chronic diseases to improve the health of millions worldwide.


Why work with us?

  • We are a global team, making a social impact.
  • Competitive market salary and benefits
  • Flexible and agile working arrangements - onsite, hybrid, or WFH (dependent on location)
  • Strong and diverse Learning & Development opportunities including exposure to scientific leadership.
  • A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities, and other fun events


Key responsibilities:

  • Perform, plan coordinate and implement the following for complex studies.
  • Review statistical analysis plans and mock shells.
  • The programming, testing, and documentation of statistical programmes for creating statistical tables, figures, and listings.
  • The programming and specifications writing of SDTM datasets.
  • The programming and specifications writing of analysis datasets (derived datasets) and transfer files for internal and external clients.
  • Create meta-data representations of regulatory-specific and analysis data sets.
  • Conduct peer-review of outputs from junior statistical programmers.
  • The programming quality control checks for the source data and reports the data issues periodically.
  • Provide advanced technical expertise for complex studies in conjunction with internal and external clients and independently bring project solutions to SP teams and the Statistical Programming department.
  • Fulfill project responsibilities at the level of technical team lead for single complex studies or group of studies.
  • Directly communicate with the internal team including data management, project management, client statisticians, and client team members to ensure an appropriate understanding of requirements and project timelines.
  • Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
  • Use and promote established standards, SOPs, and best practices.


Education and Expertise:

  • Minimum Bachelor's degree in sciences science-related field.
  • 2-7 years experience with statistical programming in SAS.
  • Minimum 3 to 5 years experience in the CRO environment.
  • Technological proficiency including SAS and Microsoft Office packages.
  • Ability to see the big picture, yet still focus on detail and quality of work.
  • Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.
  • Good teamwork and willingness to help other team members.


This is an excellent opportunity to work with a growing and global CRO. We offer a competitive salary package, flexible working conditions, and strong growth and development opportunities. Please follow us on LinkedIn to learn more about your future with George Clinical.


We welcome confidential queries and are happy to have a call to discuss this and future opportunities at your convenience. Applications and enquiries for this role should be directed to . All applications will be treated confidentially.


We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.


Thank you for your interest in working with George Clinical. As a global business, we are committed to handling Personal Information in accordance with applicable privacy and data protection laws in the many countries in which we do business. Please see our Privacy Policy for further information.


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