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

Pharmacovigilance Services Associate

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Job Description

Location: Bangalore, Chennai, Trivandrum, India
Job ID: JR136991

Job Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. The company fosters an inclusive and innovative environment that values excellence and collaboration. As part of ICON’s commitment to transforming clinical research, the Clinical Data Coordinator I role supports data-driven decision-making that advances novel therapies and improves patient outcomes.

Role & Responsibilities

  • Assist the Data Management Study Lead in developing eCRFs, Data Validation Specifications, and Study-Specific Procedures.
  • Review clinical and third-party data based on edit specifications and data review plans.
  • Issue clear, accurate, and concise data queries to investigational sites.Communicate effectively with peers, clinical data scientists, and management as needed.
  • Perform essential project activities to meet study timelines, such as documentation filing, archiving, and query dispatching.

Educational Qualification

  • Bachelor’s degree in Life Sciences, Healthcare, or a related field.
  • Basic knowledge of clinical data management in the pharmaceutical or biotechnology industry.
  • Familiarity with data management systems (e.g., Medidata, Oracle RDC, or similar).
  • Strong attention to detail and the ability to thrive in a fast-paced environment.
  • Excellent communication and teamwork skills.
  • Knowledge of regulatory guidelines (ICH-GCP) is an advantage.

Location

Bangalore, Chennai, Trivandrum, India

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