Data Process Associate

0 - 2 years

2 - 4 Lacs

Posted:3 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Step into the critical role of a

Data Process Associate

and contribute to the success of clinical trials by ensuring accurate and compliant data management. This role offers you the chance to develop key skills, work alongside experienced professionals, and build a strong foundation for your future in clinical research. If you're detail-focused and driven to support meaningful healthcare advancements, this is your opportunity to grow and make a difference.

 

What You Will Do:

  • Accurately enter and verify clinical data from Case Report Forms (CRFs) into study databases following established guidelines.
  • Perform quality control checks to ensure data integrity and compliance with regulatory standards.
  • Assist in database testing, documentation preparation, and processing of clinical data for multiple projects.
  • Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation.
  • Collaborate with project managers and cross-functional teams to ensure timely delivery of data management tasks.
  • Identify opportunities to improve processes and contribute to maintaining high-quality standards.
  • Perform medical coding activities and other assigned tasks to support study completion.

What You Will Gain:

  • Hands-on experience in clinical data management within a regulated and fast-paced environment.
  • In-depth understanding of industry standards, including ICH guidelines, GCP, and data handling regulations.
  • Exposure to project management and teamwork across global, cross-functional clinical research teams.
  • Development of strong analytical, communication, and technical skills using industry-leading tools and systems.
  • A solid foundation for career growth in clinical research and data management disciplines.
  • The opportunity to contribute to impactful clinical studies that advance healthcare and patient outcomes.

Education:

  • Qualified to Masters in life sciences background

Skills, Knowledge, and Experience:

  • PC skills, including some knowledge of Excel and Word.

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Clinical Research Organization (CRO)

Peterborough

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