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Principal Stats Programmer

4 months ago

Bengaluru, India MUM Fortrea Development India Pvt Ltd Full time
Description

: -

Act as the Lead Programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)

Work on complex problems where analysis of situations or data requires an evaluation of intangible variables; development of technical solutions to abstract problems which require the use of ingenuity and creativity

Review and interpret Statistical Analysis Plans and provide comments for assigned projects. Ensure quality of personal work and the work of the programming team when acting as a Biometrics Project Manager and Lead Programmer meeting completions dates with minimal supervision

Representing Statistical Programming at internal project team meetings, client meetings and audits

Contribute to proposal activities and client presentations providing time and cost estimates for statistical programming activities

Perform ongoing review of hours for assigned projects, ensure all issues are highlighted and resolved as quickly as possible and ensure all non-contract tasks are identified, tracked and included in change order forms

Qualifications (Minimum Required):Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.

Experience and/or education plus relevant work experience, equating to a Bachelor's degree.

Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):Typically, 7 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.

Experience as lead statistical programmer on complex studies in clinical research.

Knowledge in all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.g., Biostatistics and Clinical Data Management.

Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guide and submission standards.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.