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Document Qc Specialist

IQVIA
2-3 years
INR 8-14 LPA
Bangalore, India
10 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Overview

This role supports clinical study teams by managing and maintaining Trial Master File (TMF) and clinical records throughout the study lifecycle.

The position ensures:

  • Regulatory compliance

  • TMF quality and completeness

  • Proper records retention and archival

  • Timely document retrieval

  • Records management process execution

All activities must comply with:

  • SOPs

  • ICH-GCP Guidelines

  • Regulatory Requirements

  • Company Policies

  • Project Timelines


Key Responsibilities

TMF & Records Management

  • Support study teams with TMF-related activities.

  • Maintain and organize clinical trial documentation.

  • Ensure completeness, quality, and compliance of records.

  • Administer records management systems.


Document Processing & Archiving

  • Coordinate:

    • Document imaging

    • Scanning

    • Storage

    • Retrieval

    • Retention

    • Archival

    • Disposal

  • Prepare closed studies for final archival and storage.


Compliance & Quality Oversight

  • Review filing accuracy and document quality.

  • Ensure compliance with:

    • IQVIA SOPs

    • Customer File Plans

    • Regulatory Requirements

  • Maintain records center security and integrity.


Stakeholder Support

  • Act as primary point of contact for:

    • Internal teams

    • External clients

    • Study teams

  • Support document retrieval requests.

  • Coordinate with departments to fulfill information requests.


Scanning & Electronic Records

  • Manage scanning operations.

  • Train staff on scanning procedures.

  • Ensure accurate electronic document capture and storage.


Project Coordination

  • Monitor project outputs and timelines.

  • Ensure project goals and commitments are achieved.

  • Support records management projects.


Leadership Responsibilities

  • Train team members on:

    • TMF procedures

    • Records management practices

    • SOP compliance

  • May act as Team Lead for records management activities.


Required Skills & Knowledge

Clinical Research Knowledge

Strong Understanding Of:

  • Trial Master File (TMF)

  • Clinical Trial Documentation

  • Records Management

  • Study Archival Processes


Regulatory Knowledge

Good Knowledge Of:

  • ICH Guidelines

  • Good Clinical Practice (GCP)

  • Clinical Research Regulations

  • Local Regulatory Requirements

  • Records Retention Requirements


Technical Skills

  • Electronic Document Management Systems (EDMS)

  • TMF Systems

  • Microsoft Office Suite

  • Data Entry & Validation

  • Records Management Technologies


Soft Skills

  • Attention to Detail

  • Organizational Skills

  • Time Management

  • Problem Solving

  • Decision Making

  • Communication Skills

  • Team Leadership

  • Stakeholder Management


Physical & Work Environment Requirements

Role May Require:

  • Long periods of:

    • Sitting

    • Keyboard work

    • Documentation review

Physical Activities:

  • Standing

  • Walking

  • Reaching

  • Filing records

  • Using ladders for storage retrieval

Lifting Requirement:

  • Up to 18 Kg (40 lbs)

Working Hours:

  • May require shift-based work


Preferred Candidate Profile

Must Have

  • 3–4 years TMF or Clinical Records experience

  • Clinical Research Industry exposure

  • Knowledge of ICH-GCP

  • Records Management experience

  • Strong documentation skills

Good to Have

  • eTMF Systems Experience

  • Regulatory Inspection Readiness Experience

  • Clinical Operations Support Experience

  • Team Leadership Exposure