GSK Company hiring graduates for Programmer/Analyst role freshers can Apply Don’t miss this opportunity apply Fast!

Job Description

Company Name :-

GSK

Designation / Position :-

Programmer/Analyst

Type :-

Full-Time

Location :-

Banglore India.

About the comapny :-

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. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Qualification :-

Any Degree

Experience:-

Freshers

All Details:-

This specialized Programmer/Analyst role combines technical proficiency with leadership and project management skills to provide timely, high-quality and compliant deliverables to support Oncology Disease Data Strategy (DDS) Objectives under supervision. Programmer/Analysts are expected to be subject matter experts and be able to mentor and train junior team members and new hires. They possess good communication and time management skills, are problem solvers, be able to engage in study lead responsibilities, and are willing to mentor junior programmers and new hires. This role also requires proactive cross-functional engagement with stakeholders, end-to-end disease area expertise, and a strong commitment to quality and innovation in statistical programming. Programmer/Analysts will be expected to participate in capabilities and non-project initiatives, present at internal forums, and learn new programming languages. They will also interact with non-programming team members and participate in core study team meetings under supervision.In this role you willPerform the transformation and harmonization of existing or acquired data (e.g., external and GSK Historical Trial Data (HTD), Real World Data (RWD), Biomarker) to drive the investigations required to meet the priority disease area objectivesDevelop and maintain a deep understanding of the Oncology disease area, data sources and advocate for quality deliverables and compliance with standardsAuthor or advise on parts of the disease strategy analytics plan and relevant associated documentsProactively seek implementation of new tools in for exploratory analysis of acquired and internal dataDevelop strong relationships with statisticians and team members.Keep an awareness of departmental strategies and initiativesProvide input to strategic planning, where requested and under supervision, which may be shared with stakeholdersAnticipate problems related to assigned work or areas of expertise and able to implement solutions, proactively seeking input from colleagues as neededProvide innovative solutions to solve more complex problems relating to own workUnderstand GxP, ICH requirements, internal processes and external regulations that govern drug development (where applicable)Demonstrate effectiveness in oral and written communications, ability to express ideas, and incorporate feedback to produce quality deliverables

Key Details:-

We are looking for professionals with these required skills to achieve our goals:A BSc or BA (or equivalent) in Mathematics, Statistics, Computer Science or related subjectIntermediate to advanced programming skills in one or more programming languages, such as R, Python, and/or SASFamiliarity with CDISC standards and its applicationBasic knowledge of Microsoft Office software (MS Word, Excel, PowerPoint, Outlook)Preferred Qualifications & Skills:Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:Experience with reuse of various forms of data such as Historical Trial data, Real World Data, Biomarker from various sourcesExperience with the concept of data reuse and External Control ArmsExperience with writing and applying Metadata Specifications/Derivations.Intermediate to advanced understanding of the end-to-end clinical trial processStrong understanding of the purpose and application of key clinical documentsEffective written, verbal communication skillsBasic experience with representing programming function in cross-functional meetings, initiatives, and working groups.Some experience with training and mentoring junior programmersTherapeutic area expertise – Oncology preferred

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