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

Pharmacovigilance Services Associate

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Job Description

Location: Secunderabad, India

 Job ID: 2249

Introduction

 Certara accelerates medicines using proprietary biosimulation software, technology, and services to transform drug discovery and development. Our clients include over 2,000 biopharmaceutical companies, academic institutions, and regulatory agencies across 62 countries.

We are the largest Clinical Pharmacology & Pharmacometric organization globally, offering diverse career pathways aligned with the ambitions and interests of our employees. Certara delivers value by integrating advanced simulation approaches into critical drug development deliverables to inform decision-making and strengthen regulatory submissions. Leveraging extensive experience across thousands of projects, we bring a strong track record and broad expertise to every assignment.

Role & Responsibilities

  • Play a key role in developing clinical database products across therapeutic areas, including Metabolic & CV, Neuroscience, Autoimmune, Oncology, Respiratory, ensuring high quality to support Meta-analysis (Pairwise, Network, and Model-based).
  • Analyze and annotate trial design, treatments, demographics, and outcomes data (biomarker, clinical, safety, quality of life) from clinical literature (journals, conference abstracts, regulatory reviews).
  • Digitize results from graphs for outcomes reported on linear, logarithmic, and semi-log scales with precision.
  • Maintain consistent, high-quality data processing and annotation standards.
  • Collaborate with lead consultants, peer data analysts, and Quality Managers to understand and contribute to database rules, specifications, and quality processes.
  • Participate in relevant training programs (Statistics, R coding, Systematic Literature Review, Data Analysis) and apply learnings to enhance skill development and career growth within the organization.

Educational Qualification

  • Master’s degree in Pharmacology, Pharmaceutics, Clinical Practice, Public Health, or Epidemiology; PharmD also acceptable.
  • 1–2 years of experience in Information Science, Systematic Literature Review, Health Economics, Public Health, or the Pharmaceutical Industry (preferred).
  • Strong knowledge of pharmacology and clinical research.
  • Familiarity with clinical development phases, PICOS approach, trial designs, and pharma industry data standards/ontologies.
  • Knowledge of statistics and data management tools (e.g., R) is an added advantage.

Location

 Secunderabad, India

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