IQVIA Hiring Clinical Research Associate Job in Thane for clinical research monitoring role with GCP experience. Apply before March 20, 2026.
Clinical research professionals looking to advance their careers in the pharmaceutical and healthcare research sector have a valuable opportunity with IQVIA. The organization is currently recruiting for the position of Clinical Research Associate (CRA 2) in Thane, Maharashtra. This role is suitable for candidates with experience in clinical trial monitoring and knowledge of global regulatory guidelines such as Good Clinical Practice (GCP) and ICH standards.
The selected candidate will play an important role in overseeing clinical trial activities at research sites. The position involves monitoring study progress, ensuring protocol compliance, supporting site teams, and maintaining documentation related to clinical studies. Professionals who enjoy working in a structured research environment and collaborating with healthcare teams may find this role highly rewarding. IQVIA Hiring Clinical Research Associate Job
Company Overview
IQVIA is a globally recognized organization that provides advanced clinical research services, data analytics, and healthcare intelligence solutions. The company works closely with pharmaceutical, biotechnology, and medical device organizations to support drug development and commercialization.
With a strong global presence, IQVIA combines technology, data science, and industry expertise to improve healthcare outcomes. The organization assists clients in conducting clinical trials, analyzing healthcare data, and delivering innovative solutions that support medical research and patient care. Professionals working at IQVIA often gain exposure to international clinical research practices and regulatory standards. IQVIA Hiring Clinical Research Associate Job
Job Overview
| Job Detail | Information |
|---|---|
| Company | IQVIA |
| Position | CRA 2 (Clinical Research Associate) |
| Job Location | Thane, Maharashtra, India |
| Employment Type | Full Time |
| Department | Clinical Research / Clinical Trials |
| Experience Required | Minimum 1 year On-Site Monitoring Experience |
| Education | Bachelor’s Degree in Scientific Discipline or Healthcare |
| Application Mode | Online Application |
| Job Requisition ID | R1527417 |
| Last Date to Apply | March 20, 2026 |
| Salary | As per company norms |
Job Location & Employment Type
- Location: Thane, Maharashtra, India
- Employment Type: Full-Time
- Work Nature: Clinical research monitoring and site management
This role involves coordinating with clinical trial sites and ensuring that research studies follow regulatory and protocol requirements. IQVIA Hiring Clinical Research Associate Job
Open Position / Department Details
The opening is within the Clinical Research Operations department, which is responsible for managing clinical trials and ensuring studies are conducted according to approved protocols and regulatory guidelines.
Clinical Research Associates in this team monitor study sites, support investigators, and maintain study documentation to ensure the quality and integrity of clinical trial data. IQVIA Hiring Clinical Research Associate Job
Key Roles & Responsibilities
Professionals selected for the CRA 2 role will perform several monitoring and site management responsibilities. IQVIA Hiring Clinical Research Associate Job
Clinical Site Monitoring
- Conduct site monitoring visits including site selection, initiation visits, routine monitoring, and study close-out visits.
- Ensure all monitoring activities follow Good Clinical Practice (GCP) and ICH guidelines.
- Verify that clinical trial sites comply with regulatory requirements and study protocols.
Study Site Management
- Work closely with investigators and site staff to support clinical trial execution.
- Establish consistent communication with study sites to monitor study progress.
- Provide protocol training and study-related guidance to site personnel.
Patient Recruitment and Enrollment Support
- Assist research sites in implementing subject recruitment strategies.
- Track recruitment progress and help sites meet enrollment targets for ongoing clinical studies.
- Monitor recruitment challenges and provide solutions where necessary.
Quality Assurance and Compliance
- Evaluate study site activities to ensure compliance with clinical trial protocols and regulatory standards.
- Identify and report any quality issues related to study conduct.
- Escalate concerns to appropriate study team members when required.
Documentation and Data Management
- Track study-related documentation including regulatory approvals and submissions.
- Monitor the completion and submission of case report forms (CRFs).
- Ensure timely resolution of data queries raised during the study.
Trial Master File and Investigator Documentation
- Ensure that essential site documents are properly maintained.
- Verify that documents are available for filing in the Trial Master File (TMF).
- Confirm that Investigator Site Files (ISF) meet regulatory documentation requirements.
Monitoring Reports and Follow-Up Activities
- Prepare detailed monitoring visit reports after each site visit.
- Document findings, observations, and corrective actions.
- Generate follow-up communications to study sites when required.
Collaboration with Study Teams
- Work closely with project managers, clinical teams, and other stakeholders.
- Support study start-up and operational activities when necessary.
- Assist with subject recruitment planning for assigned study sites.
Financial and Administrative Responsibilities
- Support site financial management according to clinical trial agreements.
- Assist with invoice collection and documentation when required.
IQVIA Hiring Clinical Research Associate Job
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or another scientific discipline is preferred.
- Equivalent combinations of education, training, and experience may also be considered.
Experience
- Minimum 1 year of on-site clinical monitoring experience.
- Experience in clinical research or clinical trials is required.
Skills Required
Candidates applying for this role should demonstrate several professional competencies:
- Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Understanding of clinical trial processes and regulatory compliance
- Excellent written and verbal communication skills
- Good command of the English language
- Strong organizational and problem-solving abilities
- Ability to manage time and resources effectively
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Ability to use digital devices such as laptops and mobile technology
- Capability to build professional relationships with investigators, study teams, and clients
Salary & Benefits
- Salary: As per company norms and industry standards.
Additional benefits may include professional development programs, career advancement opportunities, and exposure to global clinical research projects. IQVIA Hiring Clinical Research Associate Job
Selection Process
The hiring process generally involves several stages to evaluate candidates’ knowledge and professional skills.
Typical selection stages include:
- Online application submission
- Resume screening by the recruitment team
- HR or initial screening interview
- Technical or clinical research interview
- Final evaluation and job offer
The exact recruitment process may vary depending on company policies. IQVIA Hiring Clinical Research Associate Job
How to Apply
Interested candidates should apply through the official online application portal of the company.
Applicants should ensure their resume includes:
- Clinical trial monitoring experience
- Knowledge of GCP and ICH regulations
- Experience with site monitoring and documentation
- Relevant clinical research skills
Applying early is recommended since the application deadline is approaching soon. IQVIA Hiring Clinical Research Associate Job
Important Dates
- Last Date to Apply: March 20, 2026
Candidates are encouraged to submit their applications as soon as possible to avoid missing the deadline. IQVIA Hiring Clinical Research Associate Job
Why Apply for This Pharma Job?
This role offers an excellent opportunity for professionals looking to build a strong career in clinical research. IQVIA is known for providing exposure to international clinical trials and advanced healthcare research projects.
Key benefits of this opportunity include:
- Working with a globally recognized clinical research organization
- Gaining experience in international clinical trial standards
- Exposure to advanced healthcare research projects
- Opportunities for career growth within clinical research operations
- Building expertise in regulatory compliance and study monitoring
For candidates interested in clinical trials, drug development, and healthcare research, this position can be a strong career-building opportunity. IQVIA Hiring Clinical Research Associate Job
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that shares pharmaceutical and healthcare job updates for job seekers. We are not affiliated with IQVIA or any other company mentioned in this job post. Applicants should verify all job details on the official company website before applying. IQVIA Hiring Clinical Research Associate Job
Final Call-to-Action
Candidates with clinical research monitoring experience and knowledge of GCP guidelines should consider applying for this opportunity. Review the eligibility criteria carefully and submit your application through the official portal before the deadline. Early applications are recommended to increase the chances of being shortlisted for the recruitment process. IQVIA Hiring Clinical Research Associate Job
