Clinical Research Associate (CRA) Jobs in Bangalore & Pune | Apply Now for Clinical Trial Opportunities 2026
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(Clinical Research Associate (CRA) Jobs in Bangalore & Pune) |
Introduction
Clinical Research continues to be one of the fastest-growing career domains within the pharmaceutical and healthcare industry. Organizations involved in clinical trials are constantly looking for skilled professionals who can support study management, site coordination, monitoring activities, and regulatory compliance.
A new opportunity has been announced for Clinical Research Associate (CRA) positions in Bangalore and Pune. Candidates with at least one year of practical clinical trial experience and knowledge of site management, monitoring activities, Electronic Data Capture (EDC) systems, and clinical research workflows are encouraged to apply.
This recruitment is being conducted on a first-come, first-served basis, making it an excellent opportunity for experienced clinical research professionals who are actively seeking career advancement in the Clinical Operations domain.
If you are searching for CRA Jobs in India, Clinical Research Associate Vacancies, Clinical Trial Jobs in Bangalore, Clinical Research Careers in Pune, or CRO Jobs for Pharmacy Graduates, this article provides complete information about eligibility, responsibilities, salary expectations, application process, and career prospects.
About the Company
The hiring organization is actively involved in Clinical Research and Clinical Trial Operations, supporting study execution, site coordination, regulatory compliance, and monitoring activities. The company works closely with investigators, research sites, sponsors, and clinical teams to ensure high-quality clinical trial management.
While the official job advertisement does not disclose detailed company background information, the organization appears to operate within the Clinical Research and CRO (Contract Research Organization) sector and is currently expanding its clinical operations team across major Indian research hubs including Bangalore and Pune.
Important Note: The official company headquarters, founding year, and employee count have not been publicly disclosed in the job advertisement. Candidates are advised to verify additional company information during the recruitment process.
Job Overview Summary
The Clinical Research Associate (CRA) role is designed for professionals with basic clinical trial experience who want to advance their careers in Clinical Operations, Site Monitoring, and Clinical Trial Management.
The selected candidates will support end-to-end study activities, site management functions, investigator coordination, documentation review, EDC data management, and remote monitoring activities while ensuring compliance with ICH-GCP guidelines and study protocols.
This opportunity offers valuable exposure to modern clinical trial processes. It can serve as an important career step toward senior CRA, Lead CRA, Clinical Trial Manager, or Clinical Project Manager positions.
Vacancy Details
| Particular | Details |
|---|
| Position | Clinical Research Associate (CRA) |
| Job Type | Full-Time |
| Location | Bangalore (2 Positions), Pune (1 Position) |
| Experience Required | Minimum 1 Year |
| Preferred Joining | Immediate |
| Industry | Clinical Research / CRO |
| Application Mode | Email |
Job Role Explanation & Responsibilities
Clinical Trial Management
The Clinical Research Associate will be involved in supporting day-to-day clinical trial activities and ensuring that studies are conducted according to approved protocols and regulatory guidelines.
Site Coordination
One of the primary responsibilities includes maintaining communication with investigators, research coordinators, and clinical trial sites to ensure smooth study execution.
Monitoring Activities
Candidates will assist in site monitoring activities and review clinical trial progress to ensure compliance with study requirements.
Clinical Documentation
The role requires maintaining accurate and audit-ready documentation throughout the clinical study lifecycle.
Remote Monitoring
Modern clinical trials increasingly use remote monitoring techniques. Selected candidates will support monitoring activities using virtual tools and centralized monitoring systems.
EDC System Management
Candidates will work with Electronic Data Capture (EDC) systems to review, validate, and manage clinical trial data.
Regulatory Compliance
The CRA will help ensure compliance with:
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ICH-GCP Guidelines
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Clinical Trial Protocols
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Regulatory Requirements
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Sponsor Requirements
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Site Documentation Standards
Eligibility Criteria
Candidates must possess one of the following educational qualifications:
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M.Sc. (Life Sciences)
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B.Pharm
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M.Pharm
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BDS
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MDS
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Equivalent Life Sciences Qualification
Experience Requirement
Applicants should have:
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Minimum 1 year of Clinical Trial experience
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Site Management exposure
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Trial Coordination experience
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Knowledge of Remote Monitoring
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Experience using EDC systems
Candidates with direct site-level clinical trial exposure may receive preference during the selection process.
Skills Required
Successful candidates should possess the following skills:
Technical Skills
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Clinical Trial Management
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Site Monitoring
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Clinical Documentation
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EDC Systems
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Trial Coordination
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Clinical Data Review
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GCP Compliance
Soft Skills
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Communication Skills
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Documentation Skills
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Time Management
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Attention to Detail
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Team Collaboration
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Problem Solving
Regulatory Knowledge
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ICH-GCP Guidelines
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Clinical Research Processes
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Study Compliance Requirements
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Monitoring Standards
Salary Estimate
Although the employer has not officially disclosed the compensation package, based on current Clinical Research Associate salary trends in India for candidates with one to three years of experience, the expected salary range may be:
Estimated Salary
₹4.0 LPA – ₹7.5 LPA
Actual salary may vary depending on:
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Experience Level
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Clinical Trial Exposure
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Monitoring Experience
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Technical Skills
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Interview Performance
Additional benefits may include:
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Performance Incentives
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Career Development Programs
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Clinical Research Training
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Health Benefits
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Internal Growth Opportunities
Interview Details
Currently, no walk-in interview schedule has been announced.
Recruitment Process May Include
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Resume Screening
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HR Shortlisting
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Technical Interview
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Clinical Research Assessment
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Final Selection Discussion
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Offer Release
Candidates who can join immediately may receive preference during the hiring process.
Required Documents
Candidates should prepare the following documents before applying:
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Updated Resume/CV
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Educational Certificates
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Experience Certificates
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Current CTC Details
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Expected CTC Information
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Government ID Proof
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Passport Size Photograph
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Clinical Research Training Certificates (if available)
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GCP Certification (if available)
Job Locations
Bangalore
Bangalore remains one of India's leading clinical research and biotechnology hubs, offering numerous opportunities in CROs, pharmaceutical companies, and healthcare technology organizations.
Pune
Pune has emerged as a major center for clinical research, pharmacovigilance, regulatory affairs, and pharmaceutical development, making it an attractive destination for clinical research professionals.
How to Apply
Interested candidates should send the following details via email:
Documents Required
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Updated Resume/CV
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Current CTC
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Expected CTC
Email Address
research@tcrpl.com
Important Note
Only candidates with relevant Clinical Trial experience are encouraged to apply.
Candidates should clearly mention their preferred location (Bangalore or Pune) and highlight their clinical trial experience in the email.
Why Should You Apply?
This opportunity offers several advantages:
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Openings in both Bangalore and Pune
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Exposure to clinical trial operations
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Career growth in Clinical Research
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Opportunity to work with experienced clinical teams
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Hands-on involvement in monitoring and site management
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Strong future prospects in CRO and pharmaceutical industries
Professionals aiming to become Senior CRA, Clinical Trial Managers, Clinical Operations Leads, or Clinical Project Managers can benefit significantly from this role.
Frequently Asked Questions (FAQs)
1. Is this CRA position open for freshers?
No. Candidates must have at least one year of hands-on Clinical Trial experience.
2. Which qualifications are eligible?
B.Pharm, M.Pharm, BDS, MDS, M.Sc. Life Sciences, and equivalent qualifications are eligible.
3. What locations are available?
The openings are available in Bangalore and Pune.
4. What is the expected salary?
The estimated salary range is approximately ₹4–7.5 LPA depending on experience and skills.
5. Is knowledge of EDC systems required?
Yes. Experience with Electronic Data Capture (EDC) systems is preferred.
6. Are immediate joiners preferred?
Yes. Candidates who can join immediately may receive preference.
7. What career growth opportunities are available?
This role can lead to positions such as Senior CRA, Lead CRA, Clinical Trial Manager, Clinical Project Manager, and Clinical Operations Specialist.
Final Conclusion
The Clinical Research Associate (CRA) Jobs in Bangalore and Pune 2026 offer an excellent opportunity for professionals with clinical trial experience to advance their careers in Clinical Operations and Clinical Research.
Candidates with experience in site management, monitoring activities, EDC systems, trial coordination, and GCP compliance should strongly consider applying. The role provides valuable exposure to modern clinical trial methodologies and can serve as a foundation for long-term career growth within CROs, pharmaceutical companies, and global clinical research organizations.
For eligible candidates seeking their next step in clinical research, this opportunity represents a strong career move with promising growth potential.
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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