Fortrea Career Opportunity for TMF Classifier I in Bangalore. Apply for Life Sciences Jobs in Clinical Research Roles.
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Looking to build a successful career in the clinical research industry? This latest Fortrea Career opportunity could be the perfect step forward. Fortrea is hiring for the position of TMF Classifier I in Bangalore, offering an exciting role in Trial Master File (TMF) management and clinical documentation. Candidates searching for Life Sciences Jobs and Clinical Research Jobs can gain valuable experience working with regulatory documentation, eTMF systems, and global clinical trials in a dynamic CRO environment.

  • Position: TMF Classifier I
  • Location: Bangalore
  • Work Mode: Hybrid
  • Job Type: Full-Time

About the Company

Fortrea is a leading global contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in advancing clinical development programs. The company provides clinical trial management, patient access solutions, regulatory support, and data-driven research services across multiple therapeutic areas worldwide.

Key Responsibilities

  • Manage document classification under Smart Inbox and ARC review processes.
  • Maintain electronic Trial Master Files (eTMF) for clinical studies.
  • Conduct visual quality checks of electronic documents.
  • Perform audit-ready checks on study documentation.
  • Process and track essential study artifacts.
  • Support compliance with company SOPs, sponsor SOPs, GCP, and ICH guidelines.
  • Assist with audit preparation and corrective action implementation.
  • Participate in internal and client audits.
  • Collaborate with study teams and operational stakeholders.
  • Support continuous process improvement initiatives.

Qualifications

  • Master’s Degree with a Life Sciences.
  • Equivalent experience within clinical research environment of a minimum of 6 months to 12 months, may be substituted for education requirements.
  • Experience working in clinical electronic systems.

Skills Required

  • Clear understanding of GCP and ICH guidelines.
  • Knowledge of Regulatory/Clinical document requirements.
  • Knowledge of Microsoft Office products, web-based applications, and Adobe Acrobat Standard, plus the ability to apply related knowledge regarding scanning and other software programs.
  • Excellent interpersonal skills.

For professionals seeking Life Sciences Jobs in the clinical trial and CRO sector, this Fortrea Career opportunity offers valuable exposure to global study documentation and Trial Master File management. Candidates interested in Clinical Research Jobs can strengthen their industry experience while working in a highly regulated and quality-focused environment. Eligible applicants are encouraged to apply before the deadline.

APPLY ONLINE HERE

BioTecNika Bureau
BioTecNika Bureau is the official editorial and research desk of BioTecNika, dedicated to bringing reliable updates, career guidance, exam information, job alerts, scholarships, industry trends, and learning resources for life science and biotechnology students, researchers, and professionals. Since 2006, BioTecNika has been committed to simplifying complex scientific information and helping learners make informed academic and career decisions.

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