IQVIA Wanted Clinical Data Management Professionals

IQVIA Hiring Clinical Data Management Professionals in India – Virtual Drive

The global clinical research leader IQVIA has opened new opportunities for Clinical Data Management (CDM) professionals across India. Through a virtual interview drive scheduled for 11th and 13th March 2026, the company is inviting qualified life sciences candidates to apply for Clinical Data Specialist roles focused on Veeva EDC platforms.

This hiring drive covers multiple Indian cities including Bangalore, Hyderabad, Pune, Thane, Kochi and Kolkata. Professionals with experience in clinical data management, clinical trials data review and database management systems are encouraged to apply for this hybrid work opportunity.

Company Overview

IQVIA is one of the world’s leading clinical research organizations providing advanced analytics, clinical trial services and healthcare intelligence to pharmaceutical, biotechnology and healthcare companies. The organization plays a key role in accelerating drug development and improving patient outcomes worldwide.

With operations in more than 100 countries, IQVIA combines real world data, advanced technology and clinical research expertise to support pharmaceutical innovation and regulatory decision making. Professionals working at IQVIA contribute directly to the development and commercialization of life‑saving therapies.

Job Role and Responsibilities

Selected candidates will work as Clinical Data Specialists within the Clinical Data Management team. The role focuses on ensuring high quality clinical trial data, managing electronic data capture systems and supporting the efficient execution of clinical studies.

Key responsibilities include:

• Act as Data Operations Coordinator for assigned clinical protocols
• Support data management activities for central laboratory studies
• Review clinical trial data and perform data validation checks
• Write, track and resolve data clarification queries
• Participate in database design, testing and edit specification development
• Perform clinical data coding and ensure data consistency
• Support programming testing and database audits
• Maintain compliance with clinical data management standard operating procedures
• Collaborate with cross functional clinical research teams

These responsibilities ensure reliable clinical trial data used by pharmaceutical companies, regulatory agencies and healthcare stakeholders during drug development.

Eligibility and Educational Qualifications

Candidates applying for this Clinical Data Management role should have a background in life sciences, healthcare or related analytical disciplines.

Required education includes:

B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, Statistics, Mathematics, Biological Sciences

Additional requirements:

• Bachelor’s degree in clinical, biological or mathematical sciences or a related field
• Exposure to medical terminology and clinical research processes
• Strong analytical, organizational and communication skills
• Experience with Veeva EDC or Veeva platform preferred
• Ability to review complex clinical datasets with strong attention to detail
• Capability to work independently while collaborating with global research teams

Professionals with hands‑on experience in end‑to‑end clinical data management including study start‑up, conduct and close‑out phases will be preferred.

Location and Work Mode

Selected candidates will be based in multiple major clinical research hubs in India:

• Bangalore
• Hyderabad
• Pune
• Thane
• Kochi
• Kolkata

Work mode for this opportunity is hybrid, allowing employees to combine remote work flexibility with collaborative office interactions.

This model supports productivity while enabling professionals to work with global clinical research teams.

Application Process

Interested candidates can participate in the virtual interview drive scheduled for:

11 March 2026 (Wednesday)
13 March 2026 (Friday)

Applicants can submit their updated resume directly to the recruitment team.

Email: babymoni.changmai@iqvia.com

Candidates can also review the official job posting and apply through the company career portal:

https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Bangalore-India/Clinical-Data-Specialist_R1525503

Applicants should ensure that all information submitted during the hiring process is accurate and truthful. IQVIA maintains strict recruitment integrity policies and may disqualify candidates providing incorrect information.

Frequently Asked Questions

Who can apply for the IQVIA Clinical Data Specialist role?

Candidates with degrees in life sciences, pharmacy, biotechnology, microbiology, biochemistry, statistics or clinical research can apply.

What experience is required for this position?

Applicants should have at least 4 years of hands‑on experience in clinical data management and exposure to Veeva EDC platforms.

Is the job remote or office based?

The role follows a hybrid work model combining remote work with office collaboration.

Where are the job locations?

Positions are available in Bangalore, Hyderabad, Pune, Kochi, Thane and Kolkata.

How can candidates apply?

Candidates can email their CV to babymoni.changmai@iqvia.com or apply through the official IQVIA careers portal.

Job Summary

Category	Details
Company	IQVIA
Vacancies	Clinical Data Specialist, Clinical Data Management Professional
Required Education	B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, Statistics
Experience	4+ Years Clinical Data Management Experience
Locations	Bangalore, Hyderabad, Pune, Kochi, Thane, Kolkata
Work Mode	Hybrid
Interview Mode	Virtual Interview Drive
Drive Dates	11 March 2026 and 13 March 2026
Application	Email CV or Apply via Career Portal

Tagged as: Pharma Jobs in Bangalore, Pharma Jobs in Chennai, pharma jobs in pune