Global CRO IQVIA is hiring a Clinical Research Associate (CRA 2) in Thane, Maharashtra, India. This role is ideal for professionals with clinical trial monitoring experience and strong knowledge of ICH-GCP guidelines.
The CRA 2 role at IQVIA focuses on site monitoring, regulatory compliance, and clinical trial data integrity. The selected candidate will work closely with investigators and clinical trial sites to ensure that studies are conducted in accordance with protocol requirements, regulatory guidelines, and sponsor expectations.
Clinical Research Associate jobs are among the most sought-after careers in the clinical research and CRO industry, and this opportunity provides exposure to global clinical trials, regulatory processes, and site management activities.
Job Details
Company: IQVIA
Job Title: Clinical Research Associate 2 (CRA 2)
Location: Thane, Maharashtra, India
Job Type: Full-time
Application Deadline: 20 March 2026
Industry: Clinical Research / CRO
Key Responsibilities
The CRA 2 at IQVIA will perform monitoring and site management tasks to ensure compliance with clinical trial protocols and regulatory guidelines.
Primary responsibilities include:
โข Conduct site monitoring visits including site selection, initiation, routine monitoring, and close-out visits
โข Ensure compliance with ICH-GCP guidelines, regulatory requirements, and sponsor protocols
โข Track subject recruitment and enrollment progress to meet study milestones
โข Manage and monitor case report forms (CRF) completion and data query resolution
โข Review and maintain Trial Master File (TMF) documentation and Investigator Site File (ISF)
โข Identify and escalate quality or compliance issues at clinical trial sites
โข Prepare monitoring visit reports and follow-up documentation
โข Collaborate with cross-functional study teams for successful clinical trial execution
โข Support study start-up activities and regulatory submissions when required
โข Assist with site financial management and clinical trial agreements
Required Qualifications
Candidates applying for the IQVIA CRA 2 job in Thane should meet the following criteria:
Education
โข Bachelorโs degree in Life Sciences, Pharmacy, Nursing, or other healthcare-related discipline
Experience
โข Minimum 1 year of on-site clinical monitoring experience
Skills
โข Strong knowledge of ICH-GCP and clinical research regulations
โข Good understanding of clinical trial protocols and site monitoring processes
โข Proficiency in Microsoft Word, Excel, and PowerPoint
โข Strong communication and documentation skills
โข Ability to manage clinical trial timelines and multiple study sites
Why Work at IQVIA
IQVIA is one of the largest global Contract Research Organizations (CROs) providing clinical research services and healthcare analytics.
Benefits of working at IQVIA include:
โข Opportunity to work on global clinical trials
โข Exposure to advanced clinical research technologies and methodologies
โข Collaborative environment with global research teams
โข Career growth in clinical monitoring and clinical operations
โข Competitive compensation and benefits
How to Apply
