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Klinera Hiring Clinical Data Associate in Mumbai | CDM Jobs 2026 for B.Pharm, M.Pharm, Life Sciences Graduates
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Klinera Hiring Clinical Data Associate in Mumbai | Clinical Data Management Jobs 2026
Introduction
Clinical Data Management (CDM) remains one of the fastest-growing sectors within the clinical research industry. Professionals with expertise in Electronic Data Capture (EDC), data validation, query management, and regulatory compliance are increasingly in demand as pharmaceutical companies and CROs continue expanding their global clinical trial activities.
Klinera has announced an exciting opportunity for experienced Clinical Data Management professionals by opening applications for the position of Clinical Data Associate at its Mumbai office. Candidates with 3–6 years of experience in clinical research and data management can leverage this opportunity to work on global clinical trials while gaining exposure to international regulatory standards and advanced EDC platforms.
This recruitment drive is particularly attractive for candidates with experience in Medidata Rave, Oracle Clinical, CRF review, data cleaning, and clinical database management.
About Klinera
Klinera is a clinical research and healthcare consulting organization that supports pharmaceutical, biotechnology, and healthcare companies through data-driven clinical research solutions. The company focuses on delivering high-quality clinical operations, data management, regulatory support, and healthcare consulting services.
Klinera collaborates with global sponsors and research organizations to ensure clinical trial data integrity, regulatory compliance, and operational excellence throughout the study lifecycle.
Company Overview
Company Name: Klinera
Industry: Clinical Research & Healthcare Consulting
Headquarters: Mumbai, Maharashtra, India
Founded: Information not publicly disclosed
Employees: Estimated 50–200 professionals
Business Focus: Clinical Research, Clinical Data Management, Regulatory Support, Healthcare Consulting
Job Overview Summary
The Clinical Data Associate position at Klinera is designed for professionals who have practical experience in managing clinical trial data and ensuring data quality throughout the research process.
The selected candidate will collaborate with study teams, clinical operations personnel, database programmers, and investigators to support data collection, validation, query resolution, database maintenance, and regulatory compliance.
This role offers significant exposure to global clinical trials, advanced EDC systems, and international clinical research standards, including ICH-GCP, FDA, and EMA guidelines.
Vacancy Details
| Particular | Details |
|---|---|
| Company | Klinera |
| Position | Clinical Data Associate |
| Department | Clinical Data Management |
| Location | Vidyavihar, Mumbai |
| Experience | 3–6 Years |
| Employment Type | Full-Time |
| Work Mode | 5 Days Work From Office |
| Industry | Clinical Research |
Clinical Data Associate Job Role Explanation
A Clinical Data Associate plays a critical role in maintaining the accuracy, completeness, and reliability of clinical trial data. Since regulatory approvals depend heavily on high-quality clinical data, this position directly contributes to the success of clinical studies.
At Klinera, the selected professional will support clinical research activities by ensuring data collected from study sites meets regulatory standards and protocol requirements.
Key responsibilities include:
Clinical Data Monitoring
Monitoring incoming clinical trial data from multiple sites and ensuring accuracy across study databases.
Query Management
Identifying inconsistencies, generating queries, and coordinating with study sites for timely resolutions.
CRF Review
Reviewing Case Report Forms (CRFs) to ensure proper documentation and data consistency.
Database Support
Assisting with database setup, testing, validation, maintenance, and updates related to protocol amendments.
Regulatory Compliance
Maintaining compliance with:
- ICH-GCP Guidelines
- FDA Regulations
- EMA Regulations
- Sponsor Requirements
Data Quality Assurance
Conducting regular data reviews and cleaning activities to prepare audit-ready databases and support regulatory submissions.
Eligibility Criteria
Applicants should possess any of the following qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Clinical Research
- Nursing
- Allied Health Sciences
- Other relevant Life Sciences disciplines
Experience Required
- 3–6 Years of Clinical Data Management experience
Knowledge Required
- Clinical Data Management
- Clinical Trials
- CRF Review
- Query Management
- Data Validation
- Data Cleaning
- EDC Systems
- Medidata Rave
- Oracle Clinical
- ICH-GCP Guidelines
- FDA & EMA Regulations
Skills Required
Successful candidates should demonstrate the following skills:
Technical Skills
- Clinical database management
- EDC system expertise
- Medidata Rave proficiency
- Oracle Clinical knowledge
- Data cleaning techniques
- Query management
- Clinical trial documentation
Analytical Skills
- Critical thinking
- Data review capability
- Risk identification
- Problem-solving skills
Soft Skills
- Excellent communication
- Team collaboration
- Stakeholder management
- Time management
- Attention to detail
These competencies help Clinical Data Associates manage large volumes of clinical data while maintaining regulatory compliance and study timelines.
Salary Estimate
Although Klinera has not officially disclosed the salary package, based on similar Clinical Data Associate roles in Mumbai and industry benchmarks, the estimated compensation may range between:
₹7.5 LPA – ₹12.5 LPA
Actual salary may vary depending on:
- Years of experience
- EDC platform expertise
- Medidata Rave proficiency
- Previous clinical trial exposure
- Interview performance
- Internal compensation policies
Interview Details
The company has not officially published detailed interview information.
However, candidates may expect the following stages:
Stage 1: Resume Screening
HR team reviews qualifications and experience.
Stage 2: Technical Assessment
Questions may focus on:
- Clinical Data Management
- CRFs
- Data Cleaning
- Query Resolution
- EDC Platforms
- Medidata Rave
- Oracle Clinical
- ICH-GCP
Stage 3: HR Discussion
Assessment of communication skills, notice period, compensation expectations, and organizational fit.
Stage 4: Final Selection
Selected candidates receive offer details and onboarding instructions.
Required Documents
Candidates should keep the following documents ready:
- Updated Resume/CV
- Educational Certificates
- Experience Letters
- Latest Salary Slips
- PAN Card
- Aadhaar Card
- Passport-size Photograph
- Clinical Research Certifications (if available)
- Current CTC Details
- Expected CTC Information
- Notice Period Details
How to Apply
Interested candidates can send their updated resume to:
Email: prachi.sonawane@klinera.com
Candidates should mention:
- Current CTC
- Expected CTC
- Notice Period
- Total Clinical Data Management Experience
- Willingness to work from Vidyavihar, Mumbai (Yes/No)
Apply as early as possible to maximize selection opportunities.
Frequently Asked Questions (FAQs)
Is this position suitable for freshers?
No. Candidates must possess 3–6 years of Clinical Data Management experience.
Which EDC systems are preferred?
Experience with Medidata Rave, Oracle Clinical, and similar EDC platforms is highly preferred.
Is remote work available?
No. The role requires working from the Mumbai office five days a week.
Which qualifications are eligible?
B.Pharm, M.Pharm, Pharm.D, Biotechnology, Clinical Research, Nursing, and Life Sciences graduates can apply.
What is the estimated salary?
The expected salary may range from ₹7.5 LPA to ₹12.5 LPA depending on experience and skills.
Is regulatory knowledge required?
Yes. Candidates should understand ICH-GCP, FDA, and EMA guidelines.
Final Conclusion
The Klinera Clinical Data Associate Recruitment 2026 offers a valuable opportunity for experienced Clinical Data Management professionals seeking career growth in the clinical research industry. Candidates with expertise in Medidata Rave, Oracle Clinical, EDC systems, query management, data validation, and regulatory compliance can benefit from exposure to global clinical trials and international research standards.
For professionals aiming to strengthen their Clinical Data Management careers and work with advanced clinical research technologies, this opportunity deserves serious consideration.
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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