Associate Programmer
Published date: 2024/01/10
- Location: Bengaluru, Karnataka, India
Job
Company
Site Name: Bengaluru Luxor North Tower
Posted Date: Apr 20 2022
Ready to help shape the future of healthcare?
At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together.
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).
Develop broader technical knowledge and expertise (e.g. UNIX scripting, computing environments).
Provide technical advice, mentoring and training as relevant.
Identify recurring problems and work with
Company
Site Name: Bengaluru Luxor North Tower
Posted Date: Apr 20 2022
Ready to help shape the future of healthcare?
At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands.
With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive.
Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together.
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).
Develop broader technical knowledge and expertise (e.g. UNIX scripting, computing environments).
Provide technical advice, mentoring and training as relevant.
Identify recurring problems and work with
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