IQVIA Hiring for Clinical Research Coordinator Job in Bangalore for experienced candidates. Apply online before April 4, 2026. Limited openings available.
Introduction
A high-potential opportunity is now available for professionals looking to advance their careers in clinical research. This role is designed for candidates with hands-on experience in clinical settings who are eager to work on real-time clinical trials and patient-focused research. If you have a strong understanding of clinical procedures and regulatory practices, this position offers a dynamic and rewarding career path.
Company Overview
IQVIA is a globally recognized organization offering clinical research services, healthcare analytics, and commercial insights to the life sciences industry. The company combines data science, technology, and domain expertise to support drug development and improve patient outcomes worldwide. Working at IQVIA provides exposure to international clinical research standards and cutting-edge healthcare solutions.
Job Location & Employment Type
- Location: Bangalore, India
- Employment Type: Full-Time
- Work Environment: Clinical / Research Site
Open Positions / Department Details
- Position: Clinical Research Coordinator
- Department: Clinical Research / Site Management
- Job Requisition ID: R1531175
Job Overview (Quick Details Table)
| Category | Details |
|---|---|
| Job Role | Clinical Research Coordinator |
| Company | IQVIA |
| Location | Bangalore |
| Qualification | Bachelor’s / Diploma |
| Experience | Minimum 3 years required |
| Job Type | Full-Time |
| Industry | Clinical Research |
| Application Mode | Online |
| Last Date to Apply | April 4, 2026 |
Key Roles & Responsibilities
The Clinical Research Coordinator will be responsible for managing clinical trial activities, ensuring compliance with protocols, and maintaining high-quality patient data.
- Support investigators in planning and executing clinical research studies
- Review study protocols, CRFs, and clinical documentation systems
- Collect and submit regulatory and ethics documentation as required
- Recruit and screen participants for clinical trials
- Educate research subjects about study procedures, timelines, and expectations
- Maintain accurate source documentation and study records
- Schedule and conduct study visits and related procedures
- Collect, record, and verify clinical data ensuring accuracy and completeness
- Perform clinical procedures such as ECG, sample collection, spirometry, and vital sign monitoring
- Handle laboratory processes including sample preparation and logistics
- Monitor patient safety and report adverse events appropriately
- Address subject queries and manage communication throughout the study
- Participate in team meetings to coordinate daily study activities
- Assist in data quality checks and resolve queries
- Support audits, monitoring visits, and regulatory inspections
- Train new staff on study protocols and maintain training records
- Ensure study objectives are achieved within timelines and compliance standards
Eligibility Criteria
Education
- Bachelor’s Degree in Life Sciences, Pharmacy, Nursing, or related field
OR - High School Diploma with relevant clinical experience
Experience
- Minimum 3 years of experience in a clinical or medical environment
- Experience as a medical assistant, nurse, lab technician, or similar role preferred
Skills Required
- Strong knowledge of clinical trials and research processes
- Understanding of Good Clinical Practice (GCP) guidelines
- Hands-on experience with clinical procedures (e.g., ECG, spirometry, IV handling)
- Proficiency in MS Office tools (Word, Outlook, Access)
- Excellent interpersonal and communication skills
- High attention to detail and accuracy
- Ability to manage multiple tasks in a fast-paced environment
- Strong teamwork and coordination abilities
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include professional development, exposure to global clinical trials, and career growth opportunities
Selection Process
The recruitment process may include:
- Online application submission
- Resume shortlisting
- Technical/clinical interview
- HR discussion
- Final selection and onboarding
How to Apply
- Candidates must apply through the official IQVIA careers portal
- Ensure all details are accurate and updated before submission
Important Dates
- Last Date to Apply: April 4, 2026
Why Apply for This Pharma Job?
This role offers an excellent opportunity for experienced professionals to work directly in clinical trial execution and patient management. It provides hands-on exposure to real-world research, regulatory compliance, and advanced clinical procedures. Working with a globally recognized organization enhances your professional profile and opens doors to higher roles in clinical operations, site management, and clinical project leadership. Additionally, the experience gained in this role is highly valuable in the growing clinical research industry.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. We provide job information for educational purposes only. Candidates are advised to verify details from official sources before applying. We do not charge any fees.
Final Call-to-Action
Eligible and experienced candidates are encouraged to apply as soon as possible to secure this excellent opportunity in clinical research.
