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Parexel Hiring in CDM as Associate Clinical Data Coder (Work from Home)

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At Parexel, we are driven by a shared mission – to improve the world’s health. From clinical trials to regulatory consulting and market access, every solution we provide is rooted in a deep conviction to make a difference. Each member of our team, regardless of their role, contributes to the development of therapies that ultimately benefit patients. We approach our work with empathy, dedication, and a commitment to excellence.

When our values align, there’s no limit to what we can achieve. Join us in our mission to transform healthcare and improve lives globally.


Job Description: Associate Clinical Data Coder

Parexel is seeking an Associate Clinical Data Coder (ACDC) to join our team. In this role, you will be responsible for performing clinical data coding tasks, ensuring accuracy and compliance with regulatory standards. This is an excellent opportunity for individuals with a background in medical coding, clinical data management, or related fields to grow their career in a global clinical research organization.

Key Responsibilities:

  • Perform clinical coding mapping using coding dictionaries (e.g., MedDRA & WHODrug) and map to the nearest Low-Level Term (LLT) or Drug Name.
  • Identify ambiguous verbatim terms and issue queries in line with coding conventions.
  • Provide regular updates on work status to supervisors, primary coders, and sponsors.
  • Assist in coding tool setup for assigned trials and participate in User Acceptance Testing (UAT).
  • Report discrepancies in clinical dictionaries and document-related issues in the DBL process.
  • Ensure timely completion of tasks for assigned studies and proactively address coding-related issues.
  • Comply with corporate quality standards, SOPs, ICH-GCP guidelines, and other regulatory requirements.

Skills Required:

  • Strong attention to detail and commitment to First-Time Quality.
  • Ability to work collaboratively in a team environment.
  • Excellent interpersonal, oral, and written communication skills.
  • Fluency in English (written and oral).
  • Learning agility and a proactive approach to knowledge sharing.

Knowledge and Experience:

  • Basic understanding of medical terminology and coding dictionaries (e.g., MedDRA, WHODrug).
  • Familiarity with Clinical Trial/Data Management Systems (e.g., InForm, Rave, Veeva, DataLabs).
  • Awareness of Data Management processes and data flows.
  • Basic knowledge of regulatory requirements, including ICH-GCP.

Education:

  • Bachelor’s degree or equivalent medical qualification.
  • Relevant experience in clinical coding or data management is preferred.

Why Join Parexel?

  • Impactful Work: Contribute to the development of therapies that improve patient lives.
  • Global Collaboration: Work with a diverse, talented team across the globe.
  • Professional Growth: Access to training, development programs, and career advancement opportunities.
  • Innovative Environment: Be part of a company that values innovation and process improvement.

Application Link