Associate Programmer
2 weeks ago
Site Name:
Bengaluru Luxor North Tower
Posted Date:
Aug 3 2023
About the Job
Basic qualifications:
- Bachelor's Degree in engineering, Biotechnology, Computer Applications or related disciplines
- 4+ years' experience in SAS programming (including SQL and SAS macro language)
- Recognized expertise in SAS programming and SAS macro code development, R programming
- Effective written and verbal communication skills.
Preferred qualifications:
- Knowledge of other SAS modules (e.g. SAS/GRAPH, SAS Output Delivery System)
- Knowledge of nonSAS programming packages/languages (Phython, R, AI/ML)
- A good level of understanding of the pharmaceutical regulatory and reporting processes (e.g. 21 CFR Part 11).
- Working knowledge of CDISC data standards, primarily the creation and use of ADaM datasets
- Experience of interacting with clinical study team members
- Ability to manage conflicting demands and priorities
- Experience of the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with/for CROs, academic institutions)
Responsibilities:
- Plan and manage programming activities across multiple studies to deliver all data analysis outputs to agreed timelines and quality, (e.g., analysis datasets, tables, figures and listings for regulatory submissions and publications).
- Oversee outsourced tasks to third party vendors to meet the agreed timelines, quality and budget requirements established for the project or study.
- Implement data standards within a function, or therapeutic area in accordance with industry standards
- Responsible for programming and QC across a study/asset including submission activities adhering to relevant SOPs / policies.
- Participate in the design of other study delivery components (e.g. case report forms, study databases).
- Review and input into key study documents (e.g. SAP, CRF etc).
- Provide technical advice, mentoring and training as relevant
- The Senior Programmer acts as a support for GSK clinical trials, accountable for creating, verifying, and documenting analyses of clinical data while adhering to study protocols, analysis plans and GSK / industry standards.
GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.
Our success absolutely depends on our people.While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive.
We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.
We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
Important notice to Employment businesses/ Agencies
**GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.
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