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Senior Statistician

4-6 years
Not Disclosed
10 Dec. 20, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Statistician
Location: Bengaluru Luxor North Tower, Bangalore
Posted Date: Oct 12, 2023
Experience Required: 4 to 6 years

About GSK:
At GSK, we unite science, technology, and talent to get ahead of disease together. As a global biopharmaceutical company, our goal is to positively impact the health of billions of people and drive sustainable shareholder returns. We focus on preventing and treating disease while aiming to positively impact the health of 2.5 billion people by 2030. At GSK, our success depends on our people, and we are committed to creating an inclusive environment where everyone can thrive, grow, and make a difference.

Biostatistics (India):
With over 20 years of experience, GSK's Biostatistics group in India plays a vital role in our global teams. Our statisticians and programmers are an integral part of the therapeutic areas, contributing to the design, analysis, and reporting of clinical trials. We offer diverse, exciting, and rewarding roles with abundant career development opportunities. We seek individuals with ambition, solid technical expertise, and a passion for making a difference in patients’ lives.

About the Job:
We are looking for a Senior Statistician to join our team and contribute to the design, execution, analysis, and interpretation of clinical trials. The ideal candidate will have expertise in a broad range of statistical methodologies and the ability to build strong relationships across teams to support the development of medicines.

Basic Qualifications:

  • PhD (Statistics) or MSc (Statistics) with >4 years of relevant experience in clinical trial design and analysis.
  • Expertise in statistical methodologies such as experimental design, mixed models, Bayesian methods, and linear/nonlinear regression.
  • Strong communication and interpersonal skills with the ability to explain novel and standard methods to both statisticians and non-statisticians.
  • Excellent influencing and relationship-building skills across multiple functions and levels of the organization.

Preferred Qualifications:

  • Experience with modeling and simulation and other innovative statistical methodologies.
  • Experience in working with regulatory bodies and submitting clinical data.
  • Demonstrated technical statistical strength and innovation in clinical trial domains.
  • Ability to work effectively with CROs and coordinate across various stakeholders.
  • Strong time management skills, with the ability to prioritize tasks across multiple projects.

Responsibilities:

  • Provide statistical input for the design, analysis, reporting, and interpretation of clinical studies.
  • Influence clinical development plans, regulatory strategies, and commercial decisions.
  • Build and maintain effective relationships with internal and external partners to meet business needs.
  • Identify and implement novel statistical methodologies to enhance medicines development.
  • Keep up-to-date with the latest developments in statistics and apply them within the organization.
  • Manage conflicting priorities and develop creative solutions to challenges.

Why GSK?
At GSK, we are driven by our purpose to unite science, technology, and talent to get ahead of disease together. We offer an inclusive work environment where employees are encouraged to innovate, grow, and contribute to improving patients' lives. GSK is a place where you can thrive both professionally and personally, making an impact on a global scale.

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