Sanofi is hiring for the position of Clinical Data Specialist in Hyderabad under its Sanofi Business Operations (SBO) organization. This is a full-time opportunity for professionals with experience in clinical data management, EDC systems, data validation and quality control.
The selected candidate will work on clinical and registry data management activities, including data verification, query management, reconciliation, electronic Case Report Form (eCRF) review, user acceptance testing, metrics tracking and data-quality activities.
Sanofi Clinical Data Specialist Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Sanofi |
| Job Title | Clinical Data Specialist |
| Location | Hyderabad, India |
| Job Type | Full Time |
| Experience | 3–5 Years |
| Education | Degree in Scientific / Life Sciences Discipline |
| Industry | Pharmaceutical / Clinical Research |
| Key Area | Clinical Data Management |
| EDC Experience | Medidata RAVE or Other EDC Systems |
| Requisition ID | R2873125 |
| 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 processes and activities supporting multiple Sanofi functions, including Specialty Care, Vaccines, General Medicines, Consumer Healthcare, Contract Manufacturing, Research & Development, and Data & Digital.
SBO works with global Medical, Health Economics and Value Assessment (HEVA), and Commercial organizations while developing internal expertise and capabilities.
Job Description
The Clinical Data Specialist will support clinical and registry study data management activities by reviewing, validating and maintaining clinical data. The position focuses on data quality, discrepancy resolution, query management, reconciliation, testing and documentation.
The role requires hands-on familiarity with EDC platforms, particularly Medidata RAVE, as well as an understanding of clinical data management processes and applicable regulatory requirements.
Key Responsibilities
Clinical Data Collection and Verification
- Understand clinical data collection workflows and systems.
- Work with electronic Case Report Forms (eCRFs) in the Medidata RAVE EDC environment.
- Review collected data for consistency and completeness.
- Identify discrepancies and support their resolution.
- Perform data validation activities to help ensure reliable clinical data.
- Identify potential sources of data-quality problems.
Query Management
- Raise queries when clinical data discrepancies are identified.
- Track and manage queries through resolution.
- Maintain appropriate documentation of data issues and resolutions.
- Support data-driven quality improvement activities.
Data Review and Quality Control
- Review clinical data listings generated through SAS.
- Examine ad-hoc reports and scanned reports for accuracy.
- Perform quality control activities within the assigned scope.
- Conduct data reconciliation to support clinical data integrity.
- Ensure data validation activities produce accurate and reliable results.
User Acceptance Testing
- Perform User Acceptance Testing (UAT) for CRF changes and system updates.
- Execute assigned test cases.
- Document testing results and findings.
- Assist in identifying and following up on system or data-related issues.
Metrics and Performance Tracking
- Create form-entry and query-related metrics.
- Track eCRF review metrics.
- Monitor backlog metrics and communicate relevant information.
- Support data management performance monitoring.
- Contribute to operational excellence and compliance readiness.
Documentation and Process Development
- Provide input into Data Review Guidelines (DRG).
- Contribute to Quality Management and Control Plans.
- Prepare project documentation when required.
- Maintain accurate records of data management activities.
- Support development and improvement of clinical data management processes.
Training and Team Support
- Facilitate training for new team members.
- Create test cases for relevant activities.
- Support team initiatives and process-improvement projects.
- Share knowledge and collaborate with colleagues and stakeholders.
- Help prioritize registry study data management activities in alignment with approved processes.
Stakeholder Collaboration
The position requires effective cooperation with internal teams, peers, stakeholders and business partners.
Key stakeholder activities include:
- Understanding internal and external customer expectations.
- Aligning priorities for registry study data management activities.
- Communicating data-quality concerns and relevant findings.
- Collaborating across teams to improve data management efficiency.
- Supporting initiatives that improve clinical data management execution.
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 academic backgrounds may include:
- Life Sciences
- Pharmacy
- Biotechnology
- Biomedical Sciences
- Other relevant scientific disciplines
Candidates should also be comfortable managing multiple activities and reviewing clinical data carefully for accuracy and completeness.
Experience Requirements
Sanofi specifies:
- 3–5 years of experience with Medidata RAVE or other EDC systems.
- Previous experience in a similar position within the pharmaceutical or clinical research industry.
- Practical experience with clinical data management.
- Experience with data validation and quality-control activities.
- Familiarity with regulatory requirements and guidelines relevant to clinical data management.
Required Technical Skills
Candidates should have knowledge or experience in:
- Medidata RAVE
- Electronic Data Capture (EDC) systems
- Clinical data management
- Data validation
- Data cleaning
- Data transformation
- Data reconciliation
- Query management
- User Acceptance Testing
- Clinical data quality control
- Data review and discrepancy identification
- Data management and analysis tools
The vacancy specifically mentions tools such as:
- SQL
- SAS
- R
- Python
Knowledge of clinical data standards such as CDISC (Clinical Data Interchange Standards Consortium) and HL7 (Health Level Seven International) is also relevant.
Regulatory Knowledge
The role requires familiarity with regulatory requirements and clinical data management guidelines, including those associated with organizations such as:
- FDA
- EMA
Knowledge of applicable clinical research standards and data-management requirements is important for maintaining compliant processes.
Soft Skills
Candidates should demonstrate:
- Strong attention to detail
- Analytical thinking
- Excellent written and verbal communication
- Strong documentation skills
- Good organizational abilities
- Project management skills
- Stakeholder management
- Ability to meet deadlines
- Ability to work independently
- Ability to work effectively within a team
- Ability to maintain confidentiality of clinical data and information
- Strong problem-solving approach
Excellent written and spoken English is required.
Work Location and Job Type
Location: Hyderabad, India
Job Type: Full Time
The provided vacancy does not specify whether the position is remote, hybrid or fully office-based.
Salary / CTC
Sanofi has not disclosed the salary or CTC for the Clinical Data Specialist position in the provided job information. Candidates should confirm compensation details through the official recruitment process.
Selection Process
The detailed selection process is not specified in the provided vacancy. Candidates should follow the official Sanofi recruitment process and complete any interview, assessment or other stages communicated by the company.
How to Apply for Sanofi Clinical Data Specialist Recruitment 2026
Interested and eligible candidates can apply online through Sanofi’s official careers portal.
- Open the official Sanofi job application page.
- Check the experience, education and technical requirements.
- Submit your updated CV/resume and required details.
- Complete the online application and any additional steps requested.
- Keep your application information for future reference.
Important Details Before Applying
- The job location is Hyderabad, India.
- This is a full-time position.
- Required experience is 3–5 years with Medidata RAVE or other EDC systems.
- Candidates should have a scientific or related life sciences degree.
- Clinical data management experience is required.
- Experience with data validation, query management and reconciliation is relevant.
- Knowledge of SAS, SQL, R or Python is specified.
- Familiarity with CDISC and HL7 standards is relevant.
- Knowledge of FDA and EMA requirements is expected.
- Strong communication, documentation and organizational skills are required.
- Candidates may be required to handle confidential clinical information.
- The application deadline is December 15, 2026.
- Job requisition ID: R2873125.
Frequently Asked Questions
1. What position is Sanofi hiring for?
Sanofi is hiring for the position of Clinical Data Specialist.
2. Where is the Clinical Data Specialist job located?
The position is based in Hyderabad, India.
3. How much experience is required?
The vacancy specifies 3–5 years of experience with Medidata RAVE or other EDC systems.
4. Is Medidata RAVE experience required?
The vacancy specifically mentions experience with Medidata RAVE or other EDC systems.
5. What educational qualification is required?
Candidates should have a degree in a scientific or related life sciences discipline with substantial clinical trial data management experience.
6. What are the main responsibilities?
The role includes clinical data verification, discrepancy identification, query management, UAT, issue tracking, metrics creation, data review, quality control, reconciliation and documentation.
7. Which software or data tools are mentioned?
The vacancy mentions SQL, SAS, R and Python as relevant data management and analysis tools.
8. Does the role involve clinical data standards?
Yes. Familiarity with CDISC and HL7 is specified.
9. Does the job involve regulatory requirements?
Yes. Candidates should be familiar with clinical data management requirements and guidelines associated with regulatory bodies such as the FDA and EMA.
10. Is this a remote or hybrid position?
The provided job listing identifies Hyderabad as the location but does not specify a remote or hybrid work arrangement.
11. What is the salary for the Clinical Data Specialist role?
The salary or CTC has not been disclosed in the provided vacancy information.
12. What is the last date to apply?
The stated application deadline is December 15, 2026.
13. What is the Sanofi requisition number?
The job requisition ID is R2873125.
Important Note
Job availability, eligibility criteria, application deadlines and recruitment conditions may change. Candidates should verify the latest information on the official Sanofi careers portal before applying.