Sanofi is hiring for the position of Clinical Data QC Reviewer in Hyderabad. This is a full-time opportunity within Sanofi Business Operations for experienced professionals with a strong background in clinical data management, data validation, quality control and electronic data capture (EDC) systems.
The selected candidate will be responsible for reviewing clinical data deliverables, performing data validation, conducting user acceptance testing, managing data issues and supporting the accuracy and integrity of registry study data.
Sanofi Clinical Data QC Reviewer Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Sanofi |
| Job Title | Clinical Data QC Reviewer |
| Location | Hyderabad, India |
| Job Type | Full Time |
| Experience | 8+ Years with Medidata RAVE or other EDC systems |
| Education | Degree in Scientific / Life Sciences Discipline |
| Industry | Clinical Research / Pharmaceutical |
| Key Area | Clinical Data Management & Quality Control |
| Requisition ID | R2873123 |
| Application Deadline | December 15, 2026 |
| Salary | Not Specified |
About Sanofi Business Operations
Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India. It centralizes various processes and activities supporting areas including Specialty Care, Vaccines, General Medicines, Consumer Healthcare, Contract Manufacturing, Research & Development, and Data & Digital functions.
The organization works as a strategic and functional partner for Sanofi’s global Medical, Health Economics and Value Assessment (HEVA), and Commercial organizations.
Job Description
The Clinical Data QC Reviewer will focus on maintaining the quality, accuracy and completeness of clinical and registry data through structured quality control and validation activities.
The role involves working with clinical data management systems, reviewing data listings, testing system or CRF changes, documenting issues and supporting corrective actions. The position also requires collaboration with internal stakeholders to maintain compliance and operational quality.
Key Responsibilities
Quality Control and Data Validation
- Perform quality control reviews of deliverables according to the approved Quality Control Plan (QCP).
- Validate registry clinical data for accuracy, completeness and consistency.
- Review clinical data management deliverables and identify potential data-quality concerns.
- Check data outputs and documentation for errors or inconsistencies.
- Support activities designed to maintain clinical data integrity.
Clinical Data and EDC Systems
- Understand clinical data collection processes and associated system workflows.
- Work with electronic Case Report Forms (eCRFs) within the Medidata RAVE Electronic Data Capture (EDC) environment.
- Review data listings generated through SAS and other reporting methods.
- Evaluate ad-hoc reports and scanned reports for consistency and accuracy.
- Identify discrepancies and support appropriate resolution.
User Acceptance Testing
- Perform User Acceptance Testing (UAT) for CRF modifications and system updates.
- Execute assigned test cases according to applicable requirements and training.
- Document UAT findings and identified issues.
- Follow up on issues to ensure appropriate resolution.
- Maintain documentation associated with testing and validation activities.
Issue and Risk Management
- Maintain the project Issue Log.
- Record identified data issues and document their resolution.
- Monitor clinical data management activities to identify potential risks.
- Communicate relevant risks and opportunities for process improvement to stakeholders.
- Support corrective actions when data or process problems are identified.
Performance and Compliance
- Maintain project databases and support routine analysis of registry study data management activities.
- Track relevant data management KPIs.
- Support operational excellence and compliance readiness.
- Follow approved processes, SOPs and quality requirements.
- Contribute to initiatives designed to improve data management efficiency.
Stakeholder Collaboration
The role requires regular collaboration with internal teams, peers, stakeholders and business partners.
Key activities include:
- Aligning with internal stakeholders on registry study data management priorities.
- Supporting team objectives and organizational initiatives.
- Communicating data-quality concerns and potential risks.
- Working collaboratively to improve registry data management processes.
- Understanding and responding to internal and external customer expectations.
- Supporting cross-functional execution of data management activities.
Educational Qualification / Eligibility Criteria
Candidates should have a degree in a scientific discipline or related life sciences field along with substantial experience in clinical trial data management.
Relevant educational backgrounds may include:
- Life Sciences
- Pharmacy
- Biomedical Sciences
- Biotechnology
- Other relevant scientific disciplines
The position places significant importance on practical experience in clinical data management and validation.
Experience Requirements
The vacancy specifies:
- 8+ years of experience with Medidata RAVE or other EDC systems.
- Experience in quality control, quality assurance or data validation within the clinical research or pharmaceutical industry.
- Hands-on experience with clinical data management and validation processes.
- Experience working with clinical trial or registry data.
- Familiarity with relevant regulatory expectations and clinical research standards.
Required Technical Skills
Candidates should have knowledge and practical experience in:
- Medidata RAVE or other EDC platforms
- Clinical data management
- Registry data management
- Data validation
- Quality control
- Quality assurance
- Clinical trial and/or RWE data management
- User Acceptance Testing
- CRF testing
- Issue tracking and resolution
- Data analysis and review
- Validation protocols
- Standard Operating Procedures (SOPs)
- Regulatory requirements
Knowledge of tools such as SQL, SAS, R or Python is also specified in the vacancy.
Candidates should be capable of identifying errors in clinical datasets, troubleshooting data issues and supporting appropriate corrective actions.
Regulatory and Compliance Knowledge
The role requires familiarity with regulatory and quality standards relevant to clinical research, including:
- FDA guidelines
- EMA guidelines
- ICH guidelines
- Good Clinical Practice (GCP)
- Good Manufacturing Practice (GMP)
Understanding these requirements can help support compliant clinical data management and quality-control activities.
Soft Skills
The position requires:
- Strong attention to detail
- Analytical thinking
- Excellent written and verbal communication
- Strong documentation skills
- Organizational skills
- Project management capabilities
- Stakeholder management
- Ability to manage multiple tasks
- Ability to work within deadlines
- Problem-solving skills
- Collaborative working style
Strong English communication skills are required.
Work Location and Job Type
Location: Hyderabad, India
Job Type: Full Time
The provided vacancy does not specify remote or hybrid working arrangements.
Salary / CTC
Sanofi has not disclosed the salary or CTC for the Clinical Data QC Reviewer position in the provided job details. Candidates should confirm compensation information during the official recruitment process.
Selection Process
The detailed selection process has not been specified in the vacancy information provided. Candidates should follow the official Sanofi recruitment process and complete any assessments or interview stages communicated by the company.
How to Apply for Sanofi Clinical Data QC Reviewer Recruitment 2026
Eligible candidates can apply online through the official Sanofi careers portal.
- Open the official job application page.
- Review the eligibility criteria and responsibilities.
- Submit your updated CV/resume and required details.
- Complete the application form and any additional steps requested.
- Keep your application information for future reference.
Important Details Before Applying
- The position is based in Hyderabad.
- This is a full-time opportunity.
- Candidates should have 8+ years of experience with Medidata RAVE or other EDC systems.
- Experience in clinical data management, quality control or data validation is required.
- A scientific or life sciences degree is specified.
- Knowledge of clinical trial and/or RWE data management is relevant.
- Experience with UAT, data validation and issue management is important.
- Knowledge of SAS, SQL, R or Python is specified.
- Familiarity with FDA, EMA and ICH guidelines is required.
- Knowledge of GCP and GMP standards is expected.
- Strong English communication and documentation skills are required.
- The stated application deadline is December 15, 2026.
- Job requisition ID: R2873123.
Frequently Asked Questions
1. What position is available at Sanofi?
Sanofi is hiring for the position of Clinical Data QC Reviewer.
2. Where is the Sanofi Clinical Data QC Reviewer job located?
The position is based in Hyderabad, India.
3. How much experience is required?
The vacancy specifies 8+ years of experience with Medidata RAVE or other EDC systems.
4. What educational qualification is required?
Candidates should have a degree in a scientific or related life sciences discipline along with substantial clinical data management experience.
5. Is Medidata RAVE experience required?
The vacancy specifically asks for 8+ years of experience with Medidata RAVE or other EDC systems.
6. What are the main responsibilities?
The role includes clinical data QC review, data validation, EDC/eCRF review, SAS data listing review, UAT, test case execution, issue-log management and clinical data quality activities.
7. Is SAS knowledge required?
The role involves reviewing data listings produced in SAS, and the vacancy also lists SAS among the relevant data management and analysis tools.
8. Which programming or data tools are mentioned?
The vacancy mentions SQL, SAS, R and Python as examples of relevant data management and analysis tools.
9. Does the position involve regulatory requirements?
Yes. Familiarity with FDA, EMA and ICH guidelines, along with GCP and GMP standards, is specified.
10. Is this a remote or hybrid job?
The provided vacancy identifies Hyderabad as the location but does not specify a remote or hybrid work arrangement.
11. What is the salary for this position?
The salary or CTC has not been disclosed in the provided vacancy details.
12. What is the last date to apply?
The stated application deadline is December 15, 2026.
13. What is the job requisition number?
The requisition ID is R2873123.
Important Note
Job availability, eligibility requirements, application deadlines and recruitment conditions can change. Candidates should verify the latest information on the official Sanofi careers portal before submitting an application.