IQVIA is hiring experienced Clinical Research Associates (CRA) for Clinical Monitoring / Clinical Operations roles across major cities in India. The opportunity is suitable for candidates with 2+ years of independent CRA experience and relevant qualifications in Pharmacy, Medicine, Dentistry, or Life Sciences.
The selected candidates will be involved in clinical trial monitoring, site management, regulatory compliance, data integrity, documentation, and coordination with investigators and clinical research teams.
Job Details
| Job Details | Information |
|---|---|
| Company | IQVIA |
| Job Title | Clinical Research Associate (CRA) / Clinical Monitor |
| Department | Clinical Monitoring / Clinical Operations |
| Experience | 2+ Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BDS, BHMS, BAMS, MBBS, or relevant Master’s in Life Sciences |
| Job Location | Bangalore, Mumbai, Hyderabad, Chennai, Delhi-NCR |
| Employment Type | Full-Time |
| Work Type | Field-based / Extensive Travel |
| Travel | Up to 50–60% |
Position Overview
The Clinical Research Associate (CRA) will be responsible for supporting and monitoring clinical trials at investigative sites. The role involves working with Principal Investigators, site staff and cross-functional teams to ensure studies are conducted according to the study protocol, ICH-GCP requirements and applicable regulatory standards.
Candidates should have independent CRA/Clinical Monitor experience along with substantial experience conducting onsite monitoring visits.
Key Responsibilities
- Monitor clinical trials at assigned investigative sites.
- Conduct Interim Monitoring Visits (IMVs) and other site management activities.
- Perform Source Data Verification (SDV) and review clinical trial data for accuracy and completeness.
- Work closely with Principal Investigators and site staff.
- Ensure compliance with study protocols, ICH-GCP and applicable regulatory requirements.
- Support ethical committee submissions and related documentation.
- Identify site-level risks, issues and deviations and coordinate appropriate follow-up.
- Maintain essential clinical trial documentation and support audit readiness.
- Work with EDC, CTMS and eTMF systems.
- Coordinate with cross-functional clinical research teams.
- Ensure timely completion of monitoring activities and required reports.
- Support the overall quality and compliance of clinical studies.
Eligibility & Qualifications
Candidates should have:
- Minimum 2+ years of independent Clinical Research Associate / Clinical Monitor experience.
- Experience conducting 80+ completed onsite Interim Monitoring Visits (IMVs) in India.
- B.Pharm, M.Pharm or Pharm.D qualification.
- BDS, BHMS, BAMS or MBBS qualification may also be considered.
- Master’s degree in Life Sciences such as Biotechnology, Microbiology, Biochemistry or Clinical Research with relevant CRO monitoring experience.
- Good understanding of ICH-GCP and applicable Indian clinical research regulations.
- Experience working with clinical trial sites and investigators.
Required Skills
- Clinical trial monitoring
- Site management
- Source Data Verification (SDV)
- Interim Monitoring Visits (IMVs)
- ICH-GCP
- Clinical trial documentation
- Regulatory compliance
- EDC systems
- CTMS and eTMF
- Risk management
- Stakeholder management
- Strong communication and negotiation skills
- Good attention to detail
- Audit readiness
Experience with systems such as Medidata Rave and Oracle InForm will be useful for the role.
Therapeutic Area Experience
Experience in therapeutic areas such as the following may be relevant:
- Oncology
- Immunology
- Cardiology
- Endocrinology
- Rare Diseases
Job Location
IQVIA has opportunities for Clinical Research Associates across major Indian metro locations, including:
- Bangalore
- Mumbai
- Hyderabad
- Chennai
- Delhi-NCR
The position involves extensive travel to investigative sites.
How to Apply
Interested and eligible candidates can apply for the Clinical Research Associate (CRA) position with IQVIA.
Application Email:
ashwini.veerabhadrappa@iqvia.com
Candidates should highlight their independent CRA experience, number of completed monitoring visits, therapeutic area experience and relevant clinical research qualifications while applying.
Company: IQVIA
Position: Clinical Research Associate (CRA)
Experience: 2+ Years
Locations: Bangalore, Mumbai, Hyderabad, Chennai & Delhi-NCR
Employment Type: Full-Time