IQVIA Hiring Clinical Data Management (Associate Clinical Data Coordinator)

IQVIA Hiring Associate Clinical Data Coordinator – Clinical Data Management | Hybrid | Bengaluru, Kochi & Mumbai

IQVIA is inviting applications for the role of Associate Clinical Data Coordinator within its Clinical Data Management team. This full-time hybrid opportunity is based primarily in Bengaluru, India, with additional locations in Kochi and Mumbai. The role focuses on supporting clinical data management activities, performing data cleaning tasks, and ensuring high-quality clinical trial datasets for sponsors and research partners.

Professionals entering the clinical research field or those with early experience in clinical data management, clinical trials, and healthcare data processing will find this role particularly valuable. As part of a global healthcare intelligence organization, the Associate Clinical Data Coordinator will work closely with data managers, project teams, clinical research associates, and sponsors to ensure accurate and regulatory-compliant data collection during clinical trials.

This position offers exposure to global clinical research operations and provides a pathway for long-term career growth in clinical data management, clinical research operations, and pharmaceutical development.

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Company Overview

IQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights for the life sciences industry. The organization supports pharmaceutical, biotechnology, and medical device companies in accelerating the development and commercialization of innovative therapies.

With operations spanning more than 100 countries, IQVIA combines advanced analytics, clinical trial expertise, and healthcare technology platforms to improve patient outcomes and population health worldwide. The company is known for managing complex global clinical trials and delivering data-driven insights that support regulatory approvals and drug development strategies.

Working at IQVIA provides professionals with exposure to cutting-edge research environments and collaborative international teams that are dedicated to improving healthcare outcomes.

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Job Role & Responsibilities

The Associate Clinical Data Coordinator supports clinical data management teams in maintaining accurate clinical trial databases and ensuring data quality throughout the study lifecycle.

Clinical Data Management Support

• Assist Data Managers in managing clinical data management projects according to sponsor requirements.
• Perform routine data cleaning and validation activities to ensure accurate and reliable clinical datasets.
• Review clinical trial data to identify inconsistencies, discrepancies, and missing values.
• Maintain quality standards for all clinical data deliverables submitted to sponsors.

Project Coordination

• Support the Data Management team in tracking project progress and meeting study timelines.
• Communicate with data team leaders regarding quality of data collection and task completion.
• Participate in internal study meetings and collaborate with cross-functional teams.
• Assist in identifying project risks and help implement corrective actions when required.

Operational Compliance

• Follow internal standard operating procedures (SOPs) and training requirements.
• Ensure compliance with sponsor guidelines and clinical research regulations.
• Support audit readiness by maintaining proper documentation and data management processes.

Collaboration with Global Teams

• Work with clinical research teams, project managers, and sponsors.
• Support senior data coordinators and serve as a backup when required.
• Maintain collaborative communication across departments involved in clinical trial operations.

This role requires strong attention to detail, analytical thinking, and the ability to work in a fast-paced clinical research environment.

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Eligibility / Qualifications

Educational Qualification

Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related healthcare discipline.

Relevant Courses: B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Biomedical Sciences, Healthcare Management.

Experience

Early-career professionals or candidates with experience in clinical data management or clinical research operations are suitable for this role.

Required Skills

• Strong understanding of clinical research and data management principles.
• Knowledge of clinical trial databases and data cleaning processes.
• Strong analytical and problem-solving abilities.
• Ability to manage tasks independently with minimal supervision.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office tools including Excel, Word, and PowerPoint.
• Ability to collaborate with cross-functional teams in a global environment.

Candidates who demonstrate strong attention to data quality and clinical research compliance will perform well in this position.

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Location & Salary

Primary Location: Bengaluru, India
Additional Locations: Kochi, India and Mumbai, India
Work Model: Hybrid
Job Type: Full-Time
Requisition ID: R1524135

Salary details are not publicly disclosed. Compensation is aligned with industry benchmarks for clinical data management professionals working in global CRO organizations.

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Why This Role Matters in Clinical Research

Clinical trials generate large volumes of patient and study data that must be accurate, complete, and compliant with regulatory standards. High-quality clinical data is essential for evaluating the safety and effectiveness of new medicines.

The Associate Clinical Data Coordinator plays a critical role in ensuring that clinical trial datasets remain reliable and ready for regulatory review. Through data cleaning, validation, and project coordination activities, this role supports the development of new therapies and contributes directly to improving global healthcare outcomes.

Professionals working in clinical data management gain valuable experience that can lead to advanced roles such as Clinical Data Manager, Clinical Project Manager, Clinical Research Associate, or Data Science Specialist in healthcare research.

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Application Process

Interested candidates can apply through the official IQVIA careers portal using the link below:

Apply Here:
https://jobs.iqvia.com/en/jobs/R1524135-1

Ensure your resume highlights experience in clinical data management, clinical research processes, and healthcare data analysis.

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Frequently Asked Questions (FAQs)

1. Who can apply for the Associate Clinical Data Coordinator role at IQVIA?

Candidates with a degree in life sciences, pharmacy, biotechnology, or clinical research can apply.

2. Is this role suitable for freshers?

Yes. Early-career professionals and entry-level candidates interested in clinical data management are encouraged to apply.

3. Is the job remote or office-based?

This position follows a hybrid work model, combining office and remote work.

4. What career growth opportunities exist in clinical data management?

Professionals can progress to Clinical Data Manager, Senior Data Coordinator, Clinical Project Manager, or Clinical Research roles.

5. What type of organization is IQVIA?

IQVIA is a global clinical research organization providing healthcare intelligence, clinical development services, and data analytics solutions for the pharmaceutical industry.

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Recruitment Summary

Company	IQVIA
Vacancies	Associate Clinical Data Coordinator
Required Education	Bachelor’s Degree in Life Sciences / Pharmacy / Biotechnology
Experience	Entry Level / Early Career in Clinical Data Management

Tagged as: Pharma Jobs in Bangalore, Pharma Jobs in Chennai, Pharma Jobs in Mumbai