Full-Time
Salary: 25k to 30k
Positions: 10

Pharmacovigilance Services Associate

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Job Description

Location: Bengaluru, India
Department: Biometrics / Biostatistics
Job Type: Internship
Job ID: 2650

Overview

The Statistical Programming Intern provides statistical programming support across multiple clinical projects, primarily using SAS, to deliver key regulatory-compliant outputs. This role involves developing programming documentation, writing efficient and accurate code, and staying current with statistical programming techniques. The intern will also provide study updates to the lead programmer while performing assigned responsibilities with high quality and integrity.

Role & Responsibilities

  • Provide statistical programming support for multiple clinical research studies under the guidance of the lead programmer.
  • Assist in generating regulatory-compliant outputs for Sponsor, Regulatory, Investigator, or Safety review meetings.
  • Develop programming documentation and annotations, including specifications, following Standard Operating Procedures (SOPs).
  • Communicate issues, progress, and updates effectively and timely to the study lead.
  • Execute assigned tasks with a focus on accuracy, efficiency, and quality.
  • Collaborate effectively with cross-functional teams to ensure study deliverables are met.

Educational Qualification

  • Education: Bachelor’s or Master’s degree in a relevant science field.
  • Experience: 0–6 months of statistical programming experience in CDISC/TLF.
  • Technical Skills: Proficiency in SAS (mandatory); knowledge of R is a plus.
  • Strong analytical and problem-solving abilities.
  • Excellent attention to detail and organizational skills.
  • Good communication skills and ability to work collaboratively in a team environment.
  • Ability to prioritize tasks, solve problems, and make informed decisions.

Location

Bengaluru, India

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