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Global drug and device development services

CDC 2 / Senior CDC

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeChennai, Tamil Nadu, India

About the Job

Requirements

  • A bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
  • Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
  • Familiarity with data management software and systems, such as Medidata or Oracle RDC.
  • Knowledge of regulatory guidelines and standards, such as ICH-GCP, is a plus.

Responsibilities

  • Assist the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and Study Specific Procedures.
  • Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
  • Track and communicate the status of study and task metrics to the clinical data scientist, project team, and functional management.
  • Address data-related questions and recommend potential solutions.
  • Identify root causes to systematically resolve data issues.

Desired Qualifications

  • Knowledge of regulatory guidelines and standards, such as ICH-GCP.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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