Responsibilities of the Intern:

• Familiarize with the GSK environment – complete relevant e-learning and adhere to job-specific SOPs and POLs.
• Gain knowledge and of clear understanding of the drug development process and clinical trials.
• Familiarity with appropriate study documents (e.g. Protocol, RAP), databases, and relevant websites.
• Learn SAS programming skills.
• If with stats background, learn the application of Biostatistics in Clinical Trials and relevant SAS procedures
• Get involved in project work under supervision from team members.
• Generate figures, tables, and listings.
• Perform Stage 1 Quality Control (QC) as per GSK QC guidelines.
• Work on academic projects and produce a dissertation under the supervision of a GSK guide
• Other project or Biostatistics-India-related duties as assigned by the team leader.

Requirements:

• High degree of analytical skills.
• Fluent written and oral communication skills