Are you an experienced Clinical Data Management (CDM) professional looking for a rewarding work-from-home opportunity with one of the world’s leading clinical research organizations? 🌍 IQVIA is currently hiring Clinical Data Management professionals with 1–6 years of experience for remote positions.

If you have hands-on experience in clinical data cleaning, EDC systems, query management, and database lock activities, this is an excellent opportunity to work on global clinical trials while enjoying the flexibility of a home-based role.

About IQVIA 🏢

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the healthcare and pharmaceutical industries. Operating in more than 100 countries, IQVIA combines human data science with innovative technology to accelerate the development of life-saving medicines and healthcare solutions.

Working at IQVIA provides professionals with opportunities to collaborate on international clinical trials while building long-term careers in a flexible and innovative work environment.

Job Overview

Details	Information
Company	IQVIA
Position	Clinical Data Management (CDM) Professional
Experience	1–6 Years
Job Location	Home-Based / Remote
Industry	Clinical Research / Pharmaceuticals
Employment Type	Full-Time
Application Mode	Email Resume Submission

Key Responsibilities

As a Clinical Data Management Professional, you’ll ensure clinical trial data remains accurate, consistent, and regulatory compliant throughout the study lifecycle.

Data Cleaning & Validation

Review Electronic Case Report Forms (eCRFs)
Perform data validation checks
Ensure data accuracy and completeness
Follow Data Management Plan (DMP)

Query Management

Generate and resolve data queries
Coordinate with investigators and study sites
Track outstanding discrepancies
Maintain audit-ready documentation

Electronic Data Capture (EDC)

Experience in one or more of the following is highly desirable:

Medidata RAVE
Oracle InForm
Veeva Vault CDM
Other industry-standard EDC platforms

Medical Coding Support

Collaborate with coding teams for:

Adverse Events (AE)
Medical History
Concomitant Medications

using:

MedDRA
WHO Drug Dictionary

Database Lock Activities

Participate in:

SAE reconciliation
External lab reconciliation
Data review
Final database lock
Quality checks

Regulatory Compliance

Ensure adherence to:

ICH-GCP Guidelines
GCDMP Standards
SOPs
Study Protocols
Client Requirements

Eligibility Criteria

Applicants should possess:

Education

B.Pharm
M.Pharm
B.Sc
M.Sc
Biotechnology
Life Sciences
Nursing
Clinical Research
Related healthcare disciplines

Experience

1–6 years in Core Clinical Data Management
Practical experience with clinical trial data
Hands-on EDC experience

Skills Required

eCRF Review
Data Cleaning
Query Management
Database Lock
Data Validation
Good Documentation Practice
Strong Communication Skills
Attention to Detail

Important Note ⚠️

Candidates whose experience is only in eTMF or only in Pharmacovigilance (PV) are not eligible for this opportunity.

Recruiters are specifically looking for professionals with core Clinical Data Management experience.

Why Join IQVIA?

Working remotely with IQVIA offers several career advantages:

Flexible Work Environment

100% Home-Based role
Better work-life balance
Reduced commuting time

Global Exposure

Collaborate with:

Clinical Project Managers
Biostatisticians
Clinical Research Associates
Global Sponsors
International Study Teams

Career Growth

IQVIA provides:

Continuous Learning Programs
Professional Certifications
Internal Promotions
Leadership Development
Global Career Opportunities

Inclusive Work Culture

Employees benefit from:

Collaborative Teams
Diverse Workforce
Innovation-Driven Environment
Employee Development Programs

How to Apply

Interested candidates can apply by following these simple steps:

Step 1

Update your resume highlighting:

CDM Experience
EDC Platforms
Clinical Trial Experience
Database Lock Activities
Therapeutic Areas
Key Achievements

Step 2

Use the following email subject:

Application for CDM Role – Your Name – X Years Experience

Step 3

Attach your updated Resume (PDF/DOCX).

Step 4

Send your application to:

imran.patel2@iqvia.com

Resume Tips to Increase Shortlisting Chances

To improve your chances of getting shortlisted, make sure your resume includes:

Medidata RAVE
Oracle InForm
Veeva Vault CDM
eCRF Review
Query Resolution
Data Cleaning
Database Lock
SAE Reconciliation
External Lab Reconciliation
MedDRA Coding
WHO Drug Dictionary
Phase I–IV Trial Experience
Therapeutic Areas
ICH-GCP
GCDMP

Whenever possible, quantify your achievements by mentioning:

Number of studies handled
Query resolution timelines
Database lock participation
Audit readiness
Data quality metrics

Why This Opportunity Stands Out

Remote Clinical Data Management roles with leading CROs like IQVIA are highly sought after because they offer the flexibility of working from home while contributing to global clinical trials. Professionals gain exposure to cutting-edge technologies, international study teams, and diverse therapeutic areas, making this an excellent opportunity for career advancement in clinical research.

If you meet the eligibility criteria, don’t miss this chance to join one of the world’s most respected clinical research organizations.

Frequently Asked Questions (FAQs)

Is this a Work From Home job?

Yes. This is a Home-Based (Remote) opportunity.

What experience is required?

Candidates should have 1–6 years of core Clinical Data Management experience.

Are freshers eligible?

No. This position requires prior hands-on CDM experience.

Can Pharmacovigilance professionals apply?

No. Candidates with only Pharmacovigilance or eTMF experience are not eligible.

How should I apply?

Email your updated resume to imran.patel2@iqvia.com with the recommended subject line.

IQVIA Hiring: Clinical Data Management (CDM) Professionals | Work From Home