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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.
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
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.
| 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 |
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:
Monitoring incoming clinical trial data from multiple sites and ensuring accuracy across study databases.
Identifying inconsistencies, generating queries, and coordinating with study sites for timely resolutions.
Reviewing Case Report Forms (CRFs) to ensure proper documentation and data consistency.
Assisting with database setup, testing, validation, maintenance, and updates related to protocol amendments.
Maintaining compliance with:
Conducting regular data reviews and cleaning activities to prepare audit-ready databases and support regulatory submissions.
Applicants should possess any of the following qualifications:
Successful candidates should demonstrate the following skills:
These competencies help Clinical Data Associates manage large volumes of clinical data while maintaining regulatory compliance and study timelines.
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:
The company has not officially published detailed interview information.
However, candidates may expect the following stages:
HR team reviews qualifications and experience.
Questions may focus on:
Assessment of communication skills, notice period, compensation expectations, and organizational fit.
Selected candidates receive offer details and onboarding instructions.
Candidates should keep the following documents ready:
Interested candidates can send their updated resume to:
Email: prachi.sonawane@klinera.com
Candidates should mention:
Apply as early as possible to maximize selection opportunities.
No. Candidates must possess 3–6 years of Clinical Data Management experience.
Experience with Medidata Rave, Oracle Clinical, and similar EDC platforms is highly preferred.
No. The role requires working from the Mumbai office five days a week.
B.Pharm, M.Pharm, Pharm.D, Biotechnology, Clinical Research, Nursing, and Life Sciences graduates can apply.
The expected salary may range from ₹7.5 LPA to ₹12.5 LPA depending on experience and skills.
Yes. Candidates should understand ICH-GCP, FDA, and EMA guidelines.
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.
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