IQVIA Hiring Clinical Research Associate (CRA 2) in Thane – Apply Before 20 March 2026
IQVIA Hiring Clinical Research Associate (CRA 2) in Thane – Pharma Job Opportunity 2026
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IQVIA Hiring Clinical Research Associate (CRA 2) |
Introduction
The clinical research industry is rapidly expanding worldwide, creating new opportunities for professionals with backgrounds in pharmacy, life sciences, and healthcare. Contract Research Organizations (CROs) play a critical role in managing clinical trials and supporting pharmaceutical companies in drug development.
One of the leading global CRO companies, IQVIA, has announced a new job opening for a Clinical Research Associate (CRA 2) position in Thane, Maharashtra, India. This role is ideal for professionals who have experience in clinical trial monitoring and a strong understanding of regulatory guidelines such as ICH-GCP.
The CRA 2 position involves monitoring clinical trial sites, ensuring compliance with protocols, and maintaining data integrity throughout the study process. Candidates selected for this role will work closely with investigators, sponsors, and research teams to ensure that clinical trials are conducted ethically and efficiently.
For professionals looking to build a career in clinical research and clinical operations, this opportunity offers exposure to global clinical trials, regulatory documentation, and site management activities.
About IQVIA
IQVIA is one of the world's leading global healthcare technology and clinical research companies. The organization provides advanced analytics, technology solutions, and contract research services to pharmaceutical, biotechnology, and healthcare organizations worldwide.
The company was formed in 2016 through the merger of IMS Health and Quintiles, combining healthcare data expertise with clinical research services.
IQVIA Headquarters
Durham, North Carolina, United States
Founded
Originally founded in 1982 (Quintiles) and later merged in 2016 to form IQVIA.
Global Presence
Operates in more than 100 countries worldwide
Employees
Over 85,000 employees globally
IQVIA is widely recognized for its role in accelerating drug development, improving patient outcomes, and providing advanced healthcare insights. The company works with leading pharmaceutical companies, regulatory authorities, and healthcare institutions across the globe.
Job Overview Summary
IQVIA is currently recruiting a Clinical Research Associate (CRA 2) for its clinical operations team in Thane, Maharashtra. The CRA role is responsible for monitoring clinical trial sites, ensuring regulatory compliance, and maintaining high-quality research data.
The selected candidate will perform monitoring visits, review trial documentation, and ensure that clinical studies follow Good Clinical Practice (GCP) standards and regulatory requirements.
This position provides an excellent opportunity for professionals with clinical monitoring experience to gain exposure to international clinical research projects and work with multidisciplinary study teams.
Vacancy Details
Company: IQVIA
Job Title: Clinical Research Associate 2 (CRA 2)
Location: Thane, Maharashtra, India
Job Type: Full-time
Industry: Clinical Research / Contract Research Organization (CRO)
Application Deadline: 20 March 2026
Job Responsibilities Explanation
The Clinical Research Associate plays a crucial role in ensuring the successful execution of clinical trials. At IQVIA, the CRA 2 professional will be responsible for monitoring clinical research sites and ensuring compliance with study protocols and regulatory standards.
One of the primary responsibilities of this role is conducting site visits at different stages of the clinical trial. These include site selection visits, site initiation visits, routine monitoring visits, and close-out visits. During these visits, the CRA evaluates the site's readiness and ensures that investigators follow study procedures.
Another important responsibility involves monitoring patient recruitment and enrollment progress. Clinical trials depend heavily on timely subject recruitment, and the CRA must ensure that sites meet study milestones and recruitment targets.
The CRA also plays a key role in maintaining documentation and data accuracy. This includes reviewing case report forms (CRFs), resolving data queries, and ensuring that all clinical trial data is complete and accurate.
In addition, the CRA is responsible for maintaining essential trial documents such as the Trial Master File (TMF) and Investigator Site File (ISF). These documents are critical for regulatory inspections and audits.
If any compliance issues or protocol deviations are identified at clinical trial sites, the CRA must immediately escalate them to the study management team and ensure corrective actions are taken.
The role also involves preparing monitoring reports, collaborating with study teams, and supporting study start-up activities,s including regulatory submissions and site contracts.
Eligibility Criteria
Education
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or other healthcare-related discipline.
Experience
Minimum 1 year of on-site clinical monitoring experience.
Skills Required
Candidates applying for the CRA 2 position should possess strong technical knowledge and professional skills related to clinical research operations.
Applicants should have a solid understanding of Good Clinical Practice (GCP) guidelines and international clinical research regulations. Knowledge of clinical trial protocols, monitoring procedures, and regulatory documentation is essential for this role.
Strong communication skills are also important, as CRAs frequently interact with investigators, research coordinators, and sponsor representatives.
Candidates should be proficient in using Microsoft Office tools such as Word, Excel, and PowerPoint for documentation, reporting, and data tracking.
Time management and organizational skills are equally important, as CRAs often handle multiple clinical trial sites simultaneously and must meet strict study timelines.
Salary Estimate
The salary for a Clinical Research Associate (CRA 2) in India typically varies based on experience, company size, and project complexity.
Estimated Salary Range
6 LPA to 12 LPA (Annual Package)
Professionals working with global CRO companies like IQVIA may also receive additional benefits such as performance bonuses, travel allowances, and health insurance.
Interview Details
The interview process may include:
Online Application Screening
Technical Interview
Clinical Research Knowledge Assessment
HR Interview
Shortlisted candidates will be contacted by the IQVIA recruitment team after reviewing applications.
Required Documents
Candidates applying for this position should keep the following documents ready during the application and interview process:
Updated Resume or CV
Educational Certificates and Degree Documents
Experience Certificates
Government ID Proof
Clinical Research Training Certificates (if available)
Passport Size Photographs
These documents help recruiters verify eligibility and professional experience.
How to Apply
Interested candidates can apply directly through the official IQVIA career portal.
Application Link
Candidates are advised to apply before the application deadline and ensure that their resume highlights relevant clinical research experience.
Frequently Asked Questions (FAQs)
What does a Clinical Research Associate do?
A Clinical Research Associate monitors clinical trial sites, ensures compliance with regulatory guidelines, verifies research data accuracy, and supports the successful completion of clinical trials.
Is CRA a good career in the pharmaceutical industry?
Yes, CRA is considered one of the most promising careers in the clinical research industry with opportunities for global projects and career growth.
What qualifications are required to become a CRA?
Most companies require a bachelor's degree in pharmacy, life sciences, nursing, or related healthcare fields along with clinical research experience.
Does IQVIA hire freshers for CRA roles?
Freshers are usually hired for entry-level roles such as Clinical Trial Assistant (CTA) or Junior CRA. CRA 2 roles generally require prior monitoring experience.
Final Conclusion
The Clinical Research Associate (CRA 2) position at IQVIA offers an excellent opportunity for professionals who want to grow in the field of clinical research and clinical trial monitoring.
Working with a globally recognized CRO like IQVIA provides exposure to international clinical studies, regulatory frameworks, and advanced clinical research technologies.
Candidates with experience in site monitoring, clinical trial documentation, and regulatory compliance should consider applying for this role before the deadline. With the growing demand for clinical research professionals in the pharmaceutical industry, CRA positions continue to offer strong career growth and global opportunities.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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