IQVIA Hiring – Clinical Research Coordinator | Bangalore
IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Coordinator at its Bangalore location. This opportunity is suitable for B.Pharm and M.Pharm professionals with 3+ years of experience who are looking to advance their career in clinical research coordination and trial operations.
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🏢 Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and technology solutions. The company partners with pharmaceutical, biotechnology, and healthcare organizations to support clinical trials and real‑world evidence generation. Working at IQVIA offers professionals exposure to global clinical research standards, regulated environments, and structured study operations.
📊 Position Details
- Position: Clinical Research Coordinator
- Department: Clinical research
- Location: Bengaluru, India
- Experience: 3+ Years
- Qualification: B.Pharm, M.pharm
- Job Type: Full-Time
- Last Date to apply: 4 April 2026
📋What You Will Do – Clinical Research Coordinator at iqvia
- Assist with study data quality checks and support query resolution to ensure accurate and complete clinical data.
- Perform a range of clinical research procedures, including ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring as per study protocol.
- Record, report, and interpret study findings accurately to support the development and maintenance of a study‑specific database.
- Assist investigators in ensuring study objectives are met on time, within budget, and in compliance with protocol requirements, regulatory standards, and quality expectations.
- Provide training to new investigator site staff on study‑specific requirements.
- Audit, maintain, and track site staff training records to ensure continued compliance.
- Prepare for and participate in study monitoring visits, audits, and regulatory inspections, supporting interactions with clinical research regulatory authorities.
- Assist research sites with staffing coverage planning and scheduling to support ongoing research activities.
- Provide day‑to‑day clinical research support to investigators during study preparation and execution, including:
🎓 Who Can Apply
- Bachelor’s degree is required
OR - High School Diploma or equivalent, along with relevant experience.
- Minimum 3 years of relevant work experience in a clinical or medical setting, such as:
- Medical Assistant
- Assistant Nurse
- Laboratory Technician
- An equivalent combination of education, training, and experience may also be considered.
- Working knowledge of clinical trial conduct and Good Clinical Practice (GCP) principles.
🧠 Key Skills
The following skills are essential for this role:
- Strong understanding of clinical and medical processes
- Experience handling patient records and medical documentation
- Familiarity with clinical research or hospital workflows
- Attention to detail and regulatory compliance
- Good communication and coordination skills
⭐ Work Insight
- Join IQVIA, a world‑leading organization in clinical research and healthcare intelligence, supporting global pharmaceutical and biotechnology companies.
- The Clinical Research Coordinator role provides an opportunity to advance your career through hands‑on involvement in clinical trials, site coordination, and study operations.
- Work on international clinical trials, gaining experience across study execution, regulatory compliance, and data quality processes.
- Strengthen your expertise in Good Clinical Practice (GCP), protocol adherence, and regulatory standards within a highly compliant research setting.
🎯 Suitable For
This opportunity is ideal for:
- Medical Assistants with ≥3 years of experience
- Assistant Nurses seeking clinical research exposure
- Laboratory Technicians transitioning into research roles
- Healthcare professionals interested in clinical trials
📈 Career Path
With experience and performance, Clinical Research Coordinators can advance into roles such as:
- Senior Clinical Research Coordinator
- Clinical Research Associate (CRA)
- Clinical Trial Manager
- Clinical Operations Specialist
Experience at IQVIA also opens opportunities in global research projects.
💰 Salary Range
- Expected Salary: As per IQVIA company standards
Compensation depends on experience level, role responsibilities, and internal company policies.
💡 Application Tips
- Revise basic clinical research and GCP concepts
- Be prepared to discuss hands‑on clinical experience
- Highlight patient handling and documentation experience in your resume
- Understand the role of CRCs in clinical trials
🔗 Explore Similar Opportunities
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
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❓FAQ-Clinical Research Coordinator at iqvia
1. Who can apply for the Clinical Research Coordinator role at IQVIA?
Candidates with a Bachelor’s degree (or High School Diploma with relevant experience) and 3+ years of experience in a clinical or medical environment can apply.
2. Is this role suitable for experienced professionals?
Yes. This role is intended for professionals with prior experience in clinical research, clinical environments, or medical settings who want to advance into study coordination roles.
3. What are the main responsibilities of this role?
You will support clinical trial execution, perform clinical procedures, manage study documentation, assist investigators, coordinate site activities, and ensure GCP‑compliant study conduct
4. Does this role involve performing clinical procedures?
Yes. The role includes clinical procedures such as ECG, sample collection, spirometry, IV catheter insertion, vital signs, and study‑specific assessments.
5. Will I support subject recruitment and screening?
Yes. You will assist with patient recruitment, screening, informed consent support, subject orientation, and maintenance of screening logs.
