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

Pharmacovigilance Services Associate

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Job Description

Ā Location: Bangalore, Chennai, Trivandrum, India
Job ID: JR135693
Job Category: Clinical Data Management
Job Type: Full-Time (Office or Home-Based)

Introduction

Ā ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Clinical Data Coordinator I to join its dynamic team. In this role, you will assist in the design, analysis, and management of clinical trial data, supporting the delivery of innovative treatments and therapies. This is an exciting opportunity to develop a career in data management within a world-class research organization.

Role & Responsibilities

  • Support the Data Management Study Lead in the development of eCRFs, Data Validation Specifications, and Study-Specific Procedures.
  • Review clinical and third-party data according to edit specifications and data review plans.
  • Generate clear, concise, and accurate data queries for investigational sites.
  • Perform project-related activities to meet study timelines, including filing, archiving, and dispatching queries for resolution.
  • Communicate effectively with peers, data scientists, and functional management.

Educational Qualification

  • Education & Qualifications
    • Bachelor’s degree in Life Sciences, Healthcare, or a related field.
    • Basic understanding of clinical data management principles within the pharmaceutical or biotechnology industry.

  • Experience & Skills
    • Familiarity with data management systems such as Medidata, Oracle RDC, or similar tools.
    • Strong attention to detail and organizational skills.
    • Excellent communication and collaboration abilities in a fast-paced environment.
    • Knowledge of ICH-GCP and regulatory standards is an advantage.

Location

Bangalore, Chennai, Trivandrum, India

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