Clinical Research Coordinator Job at IQVIA
- IQVIA Hiring Clinical Research Coordinator | Bengaluru Hybrid Clinical Trials Role
- Company Overview
- Job Role & Responsibilities
- Core Clinical Responsibilities
- Patient Management & Study Execution
- Clinical Procedures & Data Collection
- Regulatory & Compliance Activities
- Coordination & Training
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What experience is required for this role?
- 2. What qualifications are required?
- 3. What are the main responsibilities?
- 4. Is this a good clinical research career?
- 5. What skills are important for selection?
- Summary Table
IQVIA Hiring Clinical Research Coordinator | Bengaluru Hybrid Clinical Trials Role
IQVIA is hiring Clinical Research Coordinator professionals for its clinical operations team in Bengaluru, India. This is a full-time hybrid opportunity for candidates with at least 3 years of experience in clinical research, patient management, and clinical trial coordination. The role focuses on site-level clinical trial execution, patient safety monitoring, and regulatory compliance, making it a high-impact position in clinical research and healthcare development.
Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and life sciences consulting. The company works with pharmaceutical, biotechnology, and healthcare organizations to accelerate drug development, optimize clinical trials, and improve patient outcomes worldwide.
With expertise in real-world evidence, clinical operations, and regulatory compliance, IQVIA plays a crucial role in bringing innovative therapies to market. The organization is known for its advanced clinical systems, global trial execution capabilities, and commitment to high-quality healthcare research.
Job Role & Responsibilities
As a Clinical Research Coordinator, you will be responsible for executing clinical trials at the site level, managing patient interactions, and ensuring compliance with Good Clinical Practice (GCP) and regulatory standards.
Core Clinical Responsibilities
- Support investigators in preparing and executing clinical studies
- Review study protocols, Case Report Forms (CRFs), and clinical documentation
- Attend study meetings and coordinate trial-related activities
- Recruit, screen, and manage patients participating in clinical trials
Patient Management & Study Execution
- Orient patients on study procedures, timelines, and protocol requirements
- Schedule and conduct study visits and clinical procedures
- Monitor patient safety and report adverse events to medical teams
- Maintain subject logs and ensure compliance with study protocols
Clinical Procedures & Data Collection
- Perform clinical procedures such as ECG, vital signs, spirometry, sample collection, and cannulation
- Record and maintain accurate clinical data in study databases
- Ensure data quality, completeness, and regulatory compliance
- Support query resolution and data validation processes
Regulatory & Compliance Activities
- Prepare and submit regulatory and ethics documentation (FDA and other authorities)
- Maintain audit-ready documentation and support inspections
- Ensure adherence to SOPs, GCP guidelines, and study protocols
Coordination & Training
- Train site staff on study protocols and procedures
- Support monitoring visits, audits, and regulatory inspections
- Assist in workload planning and coordination of research activities
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in Life Sciences or healthcare-related fields.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing, Biomedical Sciences, Clinical Research
Experience
- Minimum 3 years of experience in clinical research or medical/clinical environment
- Experience as medical assistant, nurse, or lab technician is acceptable
Skills Required
- Strong knowledge of clinical trials and GCP guidelines
- Hands-on experience in clinical procedures and patient handling
- Excellent communication and interpersonal skills
- Strong attention to detail and data accuracy
- Ability to manage multiple tasks and work in a fast-paced environment
Location & Salary
- Job Location: Bengaluru, India
- Work Mode: Hybrid
- Employment Type: Full-time
- Salary: Competitive salary aligned with clinical research coordinator roles
Application Process
Interested candidates can apply through the official IQVIA careers portal:
Apply Here: https://jobs.iqvia.com/en/jobs/R1531175-0 fileciteturn2file0
Frequently Asked Questions (FAQs)
1. What experience is required for this role?
Candidates need at least 3 years of experience in clinical research or healthcare settings.
2. What qualifications are required?
A degree in Life Sciences, Pharmacy, Nursing, or related fields is required.
3. What are the main responsibilities?
The role involves patient management, clinical trial execution, data collection, and regulatory compliance.
4. Is this a good clinical research career?
Yes. It is a high-demand role with strong career growth in clinical operations and research.
5. What skills are important for selection?
Clinical knowledge, patient handling skills, attention to detail, and regulatory awareness.
Summary Table
| Category | Details |
|---|---|
| Company | IQVIA |
| Vacancies | Clinical Research Coordinator |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), Nursing, Biomedical Sciences, Clinical Research |
| Experience | 3+ Years Clinical Research Experience |
To apply for this job please visit jobs.iqvia.com.
