WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Advertisement

Document Specialist (TMF) Job at IQVIA

Published on

IQVIA

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Bangalore

3-4 years

Verified Job

Job Expired Dont Apply
Advertisement

IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. With a focus on accelerating medical advancements, IQVIA provides intelligent insights to improve patient outcomes worldwide.

๐Ÿ“ Location: Bangalore, India
๐Ÿ“… Application Deadline: July 16, 2025
๐Ÿ”— Job ID: R1493481


Detailed Job Description

Job Overview

As a Document Specialist at IQVIA, you will support clinical trial teams by managing Trial Master Files (TMF) and ensuring compliance with Good Clinical Practice (GCP)ICH guidelines, and regulatory requirements. Your role includes document scanning, records management, and coordinating retrieval/disposition of study records.

Advertisement

Key Responsibilities

โœ” TMF Management: Assist in maintaining and updating clinical trial documents.
โœ” Records Management: Oversee document scanning, storage, and retrieval.
โœ” Compliance: Ensure adherence to SOPs, ICH-GCP, and regulatory standards.
โœ” Team Coordination: Train staff on records management and scanning processes.
โœ” Project Support: Monitor timelines and ensure efficient document workflows.
โœ” Security & Disposal: Maintain records center security and manage document disposal.

Work Environment

  • Hybrid/On-site:ย Full-time role inย Bangalore.
  • Physical Requirements:ย Lifting up toย 40 lbs (18 kgs), standing, bending, and working with high-density filing systems.
  • Shift Work:ย May be required.

Eligibility & Qualifications

Education & Experience

  • High School Diploma or equivalentย (Required).
  • 3-4 yearsย in clinical research, records management, or related field.
  • Knowledge of ICH-GCP, regulatory guidelines, and TMF processes.

Skills Required

๐Ÿ”น Attention to detail & accuracy in documentation.
๐Ÿ”น Strong organizational & time management skills.
๐Ÿ”น Proficiency in records management software.
๐Ÿ”น Excellent communication (written & verbal).
๐Ÿ”น Problem-solving & leadership abilities.


Benefits & Perks

โœ… Competitive salary & benefits package.
โœ… Career growth in a global clinical research leader.
โœ… Training & development opportunities.
โœ… Health & wellness programs.
โœ… Collaborative work environment.


How to Apply

๐Ÿ“Œ Last Date to Apply: July 16, 2025 (6 days left).

Application Link

Advertisement

Share This Job

โœ… Job Copied Successfully!

Ad Popup