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Associate Biostatistician

1+ years
Not Disclosed
10 April 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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:

Associate Biostatistician


Job Location:

Kochi, India


Company:

IQVIA


Job Type:

Full-time | Regular


Job Requisition ID:

R1475849


Role Overview:

The Associate Biostatistician supports statistical activities across the clinical development lifecycle, including the production and validation of statistical outputs, assisting in analysis plan development, and participating in trial design discussions under supervision. The role focuses on quality deliverables, effective communication, and adherence to regulatory standards.


Key Responsibilities:

  • Execute statistical tasks per guidance, ensuring accuracy and adherence to SOPs.

  • Program datasets and generate tables, listings, and figures (TLFs) with attention to format and content.

  • Attend project team meetings and provide timely updates.

  • Support documentation efforts including annotated CRFs and specifications.

  • Contribute to risk management by flagging delivery or quality issues.

  • Assist in training new staff as needed.

  • May contribute to CSRs, SAPs, statistical reviews, and protocol development under supervision.


Education & Experience:

  • Required: Bachelor's degree in Biostatistics or a related field.

  • Experience: Typically requires at least 1 year of relevant experience, or equivalent combination of education and training.


Skills & Competencies:

  • Basic knowledge of clinical trial design and statistical methods (Phase I–IV).

  • Familiarity with GCP and ICH guidelines.

  • Strong written and verbal communication skills.

  • Proficiency in SAS or similar statistical computing tools.

  • Excellent attention to detail and organizational skills.

  • Ability to manage multiple tasks and projects effectively.

  • Team-oriented, with ability to accept direction from senior staff.


What IQVIA Offers:

  • Exposure to global clinical research and healthcare intelligence projects.

  • Professional development in a high-impact industry.

  • Opportunities for training, mentorship, and career growth.


Equal Opportunity Employer:

IQVIA is committed to fostering a diverse and inclusive workplace. All qualified applicants will receive equal opportunity without regard to race, gender, disability, veteran status, or any other protected status.