IQVIA, a global leader in clinical research, healthcare intelligence, and life sciences consulting, is inviting applications for the position of Associate Clinical Data Coordinator in Bangalore, Pune, and Thane. This is an excellent opportunity for B.Pharm graduates, Life Science graduates, and clinical research professionals looking to build a career in Clinical Data Management (CDM).
Candidates with knowledge of the clinical research process, drug development lifecycle, and data management activities can apply for this exciting opportunity with one of the world’s leading Contract Research Organizations (CROs).
Job Details
| Particulars | Details |
|---|---|
| Job Title | Associate Clinical Data Coordinator |
| Company | IQVIA |
| Job Type | Full-Time |
| Locations | Bangalore, Karnataka; Pune, Maharashtra; Thane, Maharashtra |
| Department | Clinical Data Management |
| Application Deadline | June 4, 2026 |
| Job Requisition ID | R1543101 |
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services for the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare organizations worldwide in accelerating drug development and improving patient outcomes.
Key Responsibilities
The selected Associate Clinical Data Coordinator will be responsible for:
- Performing regular data cleaning activities to ensure high-quality clinical trial data.
- Supporting data management projects according to sponsor requirements.
- Assisting Data Managers in project execution and data review processes.
- Acting as backup support for Senior Data Coordinators or Data Team Leads.
- Managing assigned tasks with minimal supervision.
- Ensuring quality deliverables within project timelines.
- Collaborating with cross-functional teams, sponsors, and clinical sites.
- Participating in internal study meetings and sponsor audits.
- Tracking project progress and identifying potential risks.
- Supporting corrective actions recommended by Data Team Leads.
- Maintaining compliance with SOPs, training requirements, and company policies.
- Providing updates regarding data quality and project status.
Eligibility Criteria
Educational Qualification
Applicants should possess:
- Bachelor of Pharmacy (B.Pharm)
- Bachelor’s Degree in Life Sciences
- Other equivalent science-related degrees
Required Skills
Candidates should have:
- Basic understanding of the drug development lifecycle
- Knowledge of clinical research processes
- Familiarity with Clinical Data Management concepts
- Proficiency in Microsoft Excel, Word, Outlook, and related applications
- Strong communication and teamwork skills
- Good written and spoken English proficiency
Preferred Candidate Profile
IQVIA is looking for professionals who can:
- Work effectively in a collaborative environment
- Deliver quality clinical data management outputs
- Handle multiple project-related tasks efficiently
- Demonstrate attention to detail and accuracy
- Support audit readiness and compliance activities
Why Join IQVIA?
Working at IQVIA offers several career advantages:
- Opportunity to work with a global clinical research leader
- Exposure to international clinical trials and data management projects
- Professional growth in Clinical Data Management
- Structured learning and development programs
- Collaborative work environment
- Career advancement opportunities within the clinical research domain
Actual compensation may vary depending on qualifications, experience, skills, and location.
How to Apply
