IQVIA, one of the world’s leading Clinical Research Organizations (CROs), is hiring experienced professionals for the Site Management CRA (Inhouse CRA) role in India. This opportunity is ideal for Clinical Research Associates with at least 3 years of on-site monitoring experience who want to transition into a structured remote site management role while continuing to support global clinical trials.
The Site Management CRA (SMa CRA) works closely with investigative sites between monitoring visits, ensuring smooth trial execution, regulatory compliance, patient safety, protocol adherence, and timely data management. If you have strong knowledge of ICH-GCP, Veeva CTMS, EDC systems, protocol compliance, and remote site management, this IQVIA job offers an excellent career opportunity.
Job Overview
- Company: IQVIA
- Job Title: Site Management CRA (Inhouse CRA)
- Job Type: Full-Time
- Experience Required: Minimum 3 Years Monitoring Experience (Mandatory)
- Locations:
- Thane, Maharashtra
- Bangalore, Karnataka
- Application Deadline: 30 July 2026
- Job Requisition ID: R1555979
Key Responsibilities
As a Site Management CRA, you will:
- Lead structured remote site management activities.
- Conduct bi-weekly site management calls.
- Support study protocol and operational queries.
- Ensure informed consent compliance.
- Monitor patient retention and adjudication activities.
- Review patient safety information.
- Support Electronic Data Capture (EDC) and CRF query resolution.
- Coordinate Investigational Medicinal Product (IMP) shipments and inventory.
- Assist sites with laboratory vendors and eCOA activities.
- Track protocol deviations and ensure corrective actions.
- Provide site training whenever required.
- Escalate study risks to Clinical Research Leads.
- Collaborate closely with Onsite CRAs.
- Maintain accurate documentation within Veeva CTMS.
- Prepare monitoring summaries and follow-up communications.
- Maintain dashboards, trackers and performance metrics.
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Nursing or other relevant Life Science discipline
Mandatory Requirements
- Minimum 3 years of CRA monitoring experience
- Strong understanding of ICH-GCP
- Experience using Veeva CTMS
- Experience with Electronic Data Capture (EDC)
- Knowledge of Case Report Forms (CRF)
- Strong communication and stakeholder management skills
- Excellent documentation practices
- Risk-based monitoring knowledge
Required Skills
- Clinical Trial Monitoring
- Site Management
- Veeva CTMS
- EDC Systems
- CRF Review
- Patient Safety
- Protocol Compliance
- ICH-GCP
- SOP Compliance
- Clinical Documentation
- Remote Site Management
- Vendor Coordination
- Clinical Operations
- Risk Assessment
- Clinical Trial Communication
Why Join IQVIA?
IQVIA is among the world’s largest providers of clinical research services and healthcare intelligence. Employees benefit from:
- Global clinical research exposure
- Career advancement opportunities
- Hybrid and remote work culture
- International study experience
- Competitive compensation
- Training and learning programs
- Exposure to advanced clinical technologies
- Opportunity to work across multiple therapeutic areas
Salary (Estimated)
Based on similar IQVIA CRA opportunities in India:
Estimated Annual Salary: โน10,00,000 โ โน16,00,000 per annum (CTC)
Actual salary depends on experience, previous compensation, interview performance and internal pay structure.
Who Should Apply?
This opportunity is ideal for professionals working as:
- Clinical Research Associate (CRA)
- Senior CRA
- Monitoring CRA
- In-house CRA
- Clinical Trial Monitor
- Site Management Associate
- Clinical Operations Executive
How to Apply
