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Document Qc Specialist

IQVIA
3-4 years
INR 5-8 LPA
Thane, 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

The role focuses on supporting clinical study teams by managing and maintaining Trial Master Files (TMF) and clinical records throughout the study lifecycle.

The candidate will be responsible for:

  • TMF maintenance and compliance

  • Clinical records management

  • Document imaging and scanning

  • Records retention and archival

  • Regulatory compliance support

  • Records retrieval and disposition activities

All activities must comply with:

  • ICH-GCP Guidelines

  • IQVIA SOPs

  • Regulatory Requirements

  • Client Quality Standards

  • Project Timelines


Key Responsibilities

TMF & Clinical Documentation Support

  • Provide TMF support to clinical study teams.

  • Maintain complete and inspection-ready trial documentation.

  • Support project execution through administrative and documentation activities.

  • Update and maintain clinical records within defined timelines.


Records Management

  • Administer records management systems.

  • Ensure proper storage, transfer, retrieval, retention, and disposal of records.

  • Coordinate recall and transfer of archived records.

  • Prepare completed studies for final archival.


Document Imaging & Scanning

  • Conduct and manage document scanning activities.

  • Train employees on scanning procedures.

  • Ensure document imaging quality and compliance.


Compliance & Quality Control

  • Monitor filing accuracy and document quality.

  • Ensure compliance with:

    • SOPs

    • Client File Plans

    • Regulatory Guidelines

  • Protect document integrity through records security controls.


Stakeholder Management

  • Serve as primary contact for:

    • Internal teams

    • External clients

    • Study stakeholders

  • Coordinate document retrieval requests.

  • Support departments requiring clinical records.


Project & Team Coordination

  • Monitor project deliverables and timelines.

  • Support records management projects.

  • Train and mentor team members.

  • May function as Team Lead for records-related activities.


Facilities & Records Operations

  • Maintain storage facilities and records infrastructure.

  • Oversee disposal of obsolete records.

  • Ensure efficient use of records storage space and equipment.


Required Skills & Knowledge

Clinical Research Knowledge

Strong Understanding Of:

  • Trial Master File (TMF)

  • Clinical Trial Documentation

  • Records Retention Processes

  • Clinical Study Lifecycle


Regulatory Knowledge

Good Knowledge Of:

  • ICH Guidelines

  • Good Clinical Practice (GCP)

  • Clinical Research Regulations

  • Local Regulatory Requirements

  • Records Management Regulations


Technical Skills

  • eTMF Systems

  • Electronic Document Management Systems (EDMS)

  • Microsoft Office Suite

  • Data Entry Systems

  • Scanning & Imaging Platforms

  • Records Management Applications


Soft Skills

  • Attention to Detail

  • Accuracy and Quality Focus

  • Time Management

  • Problem Solving

  • Organizational Skills

  • Communication Skills

  • Leadership Capability

  • Stakeholder Management


Physical & Work Environment Requirements

Role Involves

  • Extensive keyboard work

  • Significant document review

  • Long periods of sitting

Physical Activities

  • Standing

  • Walking

  • Reaching

  • Filing documents

  • Bending/Kneeling

  • Using ladders for document retrieval

Lifting Requirement

  • Up to 18 Kg (40 lbs)

Working Pattern

  • May require shift work

  • May support global teams across time zones


Preferred Candidate Profile

Must Have

  • 3–4 years Clinical Research experience

  • TMF or Records Management experience

  • Knowledge of ICH-GCP requirements

  • Strong documentation and filing skills

  • Client-facing communication abilities

Good to Have

  • eTMF System Experience

  • Inspection Readiness Experience

  • Clinical Operations Support Experience

  • Team Leadership Experience