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Job Title: Clinical Data Specialist
Company: Fortrea
Location: Bangalore, India
Employment Type: Full-time

Company Overview:
Fortrea is a leading global contract research organization (CRO) dedicated to scientific rigor and excellence in clinical development. With decades of experience in pharmaceuticals, biotechnology, and medical devices, Fortrea offers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With operations in over 90 countries and a team of over 19,000 staff, Fortrea is transforming drug and device development to benefit partners and patients worldwide.

Summary of Responsibilities:
As a Clinical Data Specialist at Fortrea, you will ensure that all allocated projects are executed in strict accordance with protocols, SOPs, and GCP standards. Your responsibilities include:

  • Reading and following study timelines for on-time deliverables.
  • Reviewing clinical trial data and raising queries to resolve errors or missing information.
  • Running additional programs to support data review activities.
  • Generating, resolving, and tracking queries to address problematic data.
  • Interacting with project team members to support Data Management aspects of projects.
  • Generating and QCing data listings for internal data review.
  • Assisting with testing of edit checks, database screen design, and functionality.
  • Supporting the completion of Database Lock and Unlock activities.
  • Training new staff on project-specific Data Management processes.
  • Performing other duties as assigned.

Qualifications (Minimum Required):

  • University/college degree in life sciences, health sciences, information technology, or related subjects, or certification in allied health professions.
  • Fluent in English, both written and verbal.

Experience (Minimum Required):

  • 3 to 5 years of relevant work experience in data management with increasing responsibility.
  • Knowledge of one or more therapeutic areas.
  • Demonstrated time management skills and ability to adhere to project timelines.
  • Knowledge of medical terminology is preferred.
  • Knowledge of effective clinical data management practices.
  • Good oral and written communication skills.

Application Link

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