IQVIA Wanted Clinical Data Management Professionals
- IQVIA Hiring Clinical Data Management Professionals | Pune & Bangalore | Work From Home Option
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Skills Required:
- Experience:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What tools are required for this role?
- Is work from home available?
- What is the career growth in this role?
- What industries are preferred?
IQVIA Hiring Clinical Data Management Professionals | Pune & Bangalore | Work From Home Option
IQVIA is currently hiring experienced professionals for Clinical Data Management roles across Pune and Bangalore, with flexible home-based work options available. This is a full-time opportunity for candidates with 3–4 years of experience in clinical data management, making it ideal for professionals looking to advance into data team lead (DTL) and project-driven roles in clinical research and CRO environments.
Multiple openings are expected within the data management function, offering strong career growth in clinical trials, regulatory data handling, and healthcare analytics.
Company Overview
IQVIA is a globally recognized leader in clinical research services, healthcare analytics, and commercial intelligence for the life sciences industry. The company partners with pharmaceutical, biotechnology, and healthcare organizations to accelerate drug development and improve patient outcomes.
With a strong presence in India and worldwide, IQVIA is known for its advanced clinical trial solutions, data-driven insights, and commitment to regulatory compliance. Working here provides exposure to global clinical projects, cutting-edge data platforms, and high-impact healthcare innovations.
Job Role & Responsibilities
As part of the Clinical Data Management team, you will handle end-to-end delivery of data management services for clinical trials. This role involves leadership responsibilities, project oversight, and ensuring high-quality clinical data aligned with regulatory standards.
Key responsibilities include:
- Manage complete clinical data management lifecycle for single or multiple studies
- Gather study setup requirements by collaborating with cross-functional stakeholders
- Perform and oversee data cleaning activities to ensure high-quality clinical datasets
- Ensure timely delivery of data management outputs within project timelines and budgets
- Act as Data Team Lead (DTL) for assigned studies
- Support validation of new device integrations and database updates
- Lead internal study meetings, sponsor calls, and audit discussions
- Monitor project progress, identify risks, and implement corrective actions
- Work closely with programming teams for automation and process improvements
- Train and mentor new team members in data management processes
- Ensure compliance with SOPs, regulatory guidelines, and quality standards
- Contribute to development and improvement of internal procedures and workflows
This role plays a critical part in ensuring accurate clinical trial data, supporting regulatory submissions, and improving drug development efficiency.
Eligibility / Qualifications
Candidates must meet the following educational requirements:
BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, Statistics, Mathematics, Bioinformatics
Skills Required:
- Strong knowledge of clinical data management and clinical trial processes
- Experience with Veeva EDC systems
- Understanding of drug development lifecycle and regulatory requirements
- Advanced skills in Microsoft Excel and data handling tools
- Strong analytical, problem-solving, and organizational skills
- Excellent communication and stakeholder management abilities
Experience:
- 3 to 4 years of clinical data management experience
- Minimum 1 year of experience in Veeva EDC
Location & Salary
- Locations: Pune, Bangalore (Work From Home / Hybrid available)
- Salary: Competitive CRO industry salary with performance-based growth
Application Process
Interested candidates can apply directly through the official IQVIA careers portal:
Apply Here: https://jobs.iqvia.com/en/jobs/R1523107-0?
Early application is recommended due to high competition for clinical research roles.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires prior experience in clinical data management.
What tools are required for this role?
Experience with Veeva EDC and strong Excel skills are important.
Is work from home available?
Yes, IQVIA offers home-based or hybrid work options depending on project requirements.
What is the career growth in this role?
Candidates can progress to roles such as Lead Data Manager, Clinical Data Lead, or Project Manager in clinical research.
What industries are preferred?
Pharmaceutical, biotechnology, CRO, and healthcare analytics experience is preferred.
| Category | Details |
|---|---|
| Company | IQVIA |
| Vacancies | Clinical Data Management (DTL / Data Management Roles) |
| Required Education | BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, Statistics, Mathematics, Bioinformatics |
| Experience | 3–4 Years |
To apply for this job please visit jobs.iqvia.com.
