IQVIA is hiring for the position of Clinical Research Associate (CRA 1/2) in Thane, Maharashtra. This is a full-time clinical research opportunity for professionals with experience in clinical trial site monitoring and study management.
The role focuses on monitoring clinical trial sites to ensure that study activities are conducted according to the approved protocol, applicable regulations, Good Clinical Practice (GCP), ICH guidelines, and sponsor requirements.
Candidates should have at least 1 year of on-site monitoring experience and preferably a bachelor’s degree in a scientific or healthcare discipline. Strong knowledge of clinical research regulations, communication skills, organization, and problem-solving ability are also required.
IQVIA Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | IQVIA |
| Job Title | CRA 1/2 |
| Full Form | Clinical Research Associate |
| Job Type | Full Time |
| Location | Thane, Maharashtra |
| Experience | Minimum 1 year of on-site monitoring |
| Qualification | Bachelor’s degree in Scientific/Healthcare discipline preferred |
| Industry | Clinical Research / Life Sciences |
| Work Area | Clinical Trial Monitoring & Site Management |
| Requisition ID | R1557317 |
| Application Deadline | October 8, 2026 |
| Salary / CTC | Not specified |
About IQVIA
IQVIA is a global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences and healthcare industries.
The company works with organizations involved in the development and commercialization of healthcare products and supports clinical research programs designed to advance medical treatments and improve patient outcomes.
Job Description
The CRA 1/2 will be responsible for monitoring assigned clinical trial sites and supporting site management activities.
The position requires the candidate to ensure that study procedures are being performed according to the clinical trial protocol, regulatory requirements, GCP/ICH guidelines, and sponsor expectations.
The CRA will also work with investigators and site teams to monitor recruitment, study documentation, data quality, regulatory submissions, and resolution of study-related issues.
Clinical Research Associate – Key Responsibilities
Site Monitoring
The CRA will conduct clinical trial monitoring visits according to the assigned project scope and regulatory requirements.
These may include:
- Site selection visits.
- Site initiation visits.
- Routine monitoring visits.
- Site close-out visits.
Monitoring activities must be performed in accordance with applicable GCP and ICH requirements.
Patient Recruitment Support
The CRA will work with clinical trial sites to develop, implement, and track subject recruitment plans.
The objective is to help sites manage recruitment according to project requirements and improve the predictability of study enrollment.
Site Training and Communication
The role includes supporting assigned sites through:
- Protocol training.
- Study-related training.
- Regular communication with site personnel.
- Management of ongoing study expectations.
- Resolution and escalation of site-related issues.
Quality and Compliance Monitoring
The CRA will evaluate whether clinical trial sites are conducting study activities appropriately.
This includes reviewing:
- Site practices.
- Protocol compliance.
- Regulatory compliance.
- Study documentation.
- Data quality and integrity.
Any significant quality concerns should be escalated through the appropriate channels.
Study Progress Tracking
The CRA will help monitor the progress of assigned clinical studies by tracking areas such as:
- Regulatory submissions and approvals.
- Patient recruitment and enrollment.
- CRF completion and submission.
- Data queries.
- Query resolution.
- Study start-up activities, where applicable.
Trial Master File and Site Files
The position includes ensuring that required site documents are available for filing in the Trial Master File (TMF).
The CRA will also verify that the Investigator Site File (ISF) is maintained according to GCP and applicable local regulatory requirements.
Monitoring Documentation
The CRA will prepare and maintain appropriate documentation relating to site management and monitoring activities.
This may include:
- Monitoring visit reports.
- Follow-up letters.
- Site action plans.
- Monitoring findings.
- Other required study documentation.
Cross-Functional Collaboration
The CRA will work closely with other members of the clinical study team to support project execution.
Effective communication with internal teams, sites, managers, clients, and other stakeholders is an important part of the position.
Additional Responsibilities
Depending on the assigned project, the CRA may also support:
- Site-level subject recruitment planning.
- Clinical trial financial management.
- Invoice retrieval according to local requirements.
- Activities related to executed clinical trial agreements.
Educational Qualification
A Bachelor’s degree in a scientific or healthcare-related discipline is preferred.
IQVIA also states that an equivalent combination of education, training, and relevant experience may be considered in place of the degree requirement.
Experience Requirements
Candidates must have at least:
1 year of on-site clinical trial monitoring experience.
Relevant experience should include practical exposure to clinical research site monitoring and study management activities.
Required Knowledge and Skills
Candidates should have good knowledge of applicable clinical research requirements, including:
- Good Clinical Practice (GCP)
- ICH guidelines
- Clinical trial protocols
- Site monitoring practices
- Clinical research processes
- Regulatory requirements
Therapeutic and Protocol Knowledge
The CRA should develop appropriate therapeutic-area and protocol knowledge through the training provided by the company.
Computer Skills
Candidates should be comfortable using:
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Laptop-based clinical research systems
- iPhone/iPad where applicable
Communication Skills
Strong written and verbal communication skills are required, along with good command of the English language.
Organizational Skills
The role requires:
- Good organizational ability.
- Problem-solving skills.
- Effective time management.
- Financial management awareness.
- Ability to manage multiple study-related activities.
Relationship Management
The candidate should be capable of establishing and maintaining effective working relationships with:
- Clinical research site teams.
- Coworkers.
- Managers.
- Clients.
- Study team members.
Work Location
Location: Thane, Maharashtra, India
Job Type: Full Time
The supplied vacancy does not specify a remote or hybrid work arrangement for this position.
Because CRA roles involve site monitoring, candidates should be prepared for travel associated with assigned clinical trial sites where required by the study.
Salary / CTC
The salary or CTC for the CRA 1/2 position has not been disclosed in the supplied job posting.
Candidates can confirm compensation and applicable employment terms during the recruitment process.
Selection Process
The supplied vacancy does not provide a detailed selection process.
Candidates may be contacted for further screening or interview stages after submitting their application, depending on IQVIA’s recruitment process.
How to Apply for IQVIA Recruitment 2026
Interested and eligible candidates can apply online through the official IQVIA careers portal.
Job Requisition ID: R1557317
Application Deadline: October 8, 2026
Candidates should ensure that all information and credentials provided in the application are accurate and complete.
Important Details Before Applying
- The position is CRA 1/2 – Clinical Research Associate.
- Location: Thane, Maharashtra.
- The role is full time.
- Minimum 1 year of on-site monitoring experience is required.
- A bachelor’s degree in a scientific or healthcare discipline is preferred.
- Equivalent education, training, and experience may be considered.
- Knowledge of GCP and ICH requirements is important.
- The position involves clinical trial site monitoring and site management.
- Responsibilities include recruitment tracking, regulatory submissions, CRF review, query management, TMF/ISF documentation, and monitoring reports.
- Strong English communication and organizational skills are required.
- Salary/CTC has not been specified.
- Application deadline: October 8, 2026.
Frequently Asked Questions
1. What is the job title at IQVIA?
The position is CRA 1/2, or Clinical Research Associate.
2. Where is the CRA job located?
The position is based in Thane, Maharashtra, India.
3. How much experience is required?
Candidates need at least 1 year of on-site monitoring experience.
4. What educational qualification is preferred?
A Bachelor’s degree in a scientific or healthcare discipline is preferred.
5. Can equivalent experience be considered instead of a degree?
Yes. IQVIA states that an equivalent combination of education, training, and experience may be accepted in place of the degree requirement.
6. What does a CRA do in this position?
The CRA monitors clinical trial sites, supports study management, checks protocol and regulatory compliance, tracks recruitment and study progress, reviews documentation, and communicates with study sites and project teams.
7. Which monitoring visits are included?
The role may involve site selection, site initiation, monitoring, and close-out visits.
8. Does the role involve GCP?
Yes. Knowledge and application of Good Clinical Practice (GCP) and relevant ICH guidelines are required.
9. Does the CRA role involve travel?
The supplied description does not provide a specific travel percentage. However, site monitoring responsibilities may require visits to assigned clinical trial sites.
10. What computer skills are required?
Candidates should be comfortable with Microsoft Word, Excel, and PowerPoint, along with laptop-based work and mobile devices where applicable.
11. What is the application deadline?
The stated application deadline is October 8, 2026.
12. What is the requisition ID?
The job requisition ID is R1557317.
13. Is salary mentioned?
No. The supplied job posting does not specify the salary or CTC.
Important Note
Recruitment requirements, application deadlines, vacancy status, and job conditions may change. Candidates should verify the latest information on the official IQVIA careers portal before applying. IQVIA also states that application information and credentials must be truthful and complete; false statements or material omissions may result in disqualification or other employment action in accordance with applicable law.