Parexel has announced a new opening for a Senior Clinical Data Analyst in Hyderabad, India. This office-based opportunity is suitable for experienced Clinical Data Management professionals with strong end-to-end study experience, including protocol review, eCRF design, database build, clinical data review, vendor management and database lock.
The Parexel Senior Clinical Data Analyst job in Hyderabad involves supporting the Data Management Lead (DML) throughout the clinical study lifecycle. Candidates with hands-on experience in Medidata RAVE, Oracle Clinical, query management, data quality review, EDC build and clinical study documentation may find this role particularly relevant.
Parexel is a global biopharmaceutical services organization supporting clinical development, regulatory, consulting and market access activities.
Job Overview
| Particular | Details |
|---|---|
| Company | Parexel |
| Job Role | Senior Clinical Data Analyst |
| Department | Clinical Data Management |
| Location | Hyderabad, India |
| Work Model | Office Based |
| Experience | 6+ Years |
| Employment | Full Time |
| Job Requisition ID | R0000044588 |
| Posted | August 11, 2026 |
| Key Systems | Medidata RAVE, Oracle Clinical |
| Industry | Clinical Research / Life Sciences |
About the Role
As a Senior Clinical Data Analyst at Parexel, the selected professional will support the Data Management Lead in planning, setup, execution, monitoring and closeout of clinical studies.
The position combines clinical database build, data review, query management, vendor oversight, study documentation, quality management and database lock activities. The Senior Clinical Data Analyst will also contribute to study metrics, Data Quality Review meetings, regulatory compliance and mentoring of junior Clinical Data Management professionals.
Key Responsibilities
Candidates selected for this Clinical Data Management job in Hyderabad may be responsible for:
- Supporting the Data Management Lead in clinical study planning, execution and project management.
- Supporting end-to-end Clinical Data Management activities from study setup through database lock.
- Preparing EDC build timelines and supporting database and edit-check specification activities.
- Performing UAT and testing for databases, coding, safety integrations and site-payment integrations.
- Coordinating clinical data review and query-management activities.
- Performing query trend analysis and supporting protocol deviation review.
- Creating, reviewing and maintaining Clinical Data Management study documentation.
- Ensuring applicable study documents are appropriately filed within the eTMF.
- Coordinating CRO, vendor and external data deliverables.
- Supporting Data Quality Review meetings and preparing relevant study metrics.
- Managing post-production activities, migrations and database-lock activities.
- Monitoring study timelines, quality indicators and Clinical Data Management deliverables.
- Supporting audit and inspection readiness.
- Working with cross-functional clinical study stakeholders.
- Ensuring activities comply with SOPs, study requirements and applicable regulatory standards.
- Providing guidance, training and mentoring to junior Clinical Data Management team members.
Qualifications and Experience
Parexel is looking for experienced professionals with approximately 6+ years of end-to-end Clinical Data Management experience.
Candidates should ideally demonstrate experience across:
Clinical Data Management: Protocol review, CRF/eCRF design, database setup, data cleaning, data review, query management and database lock.
EDC Systems: Strong working experience with Medidata RAVE and Oracle Clinical.
Data Quality: Experience in query trend analysis, protocol deviation review and overall clinical data quality oversight.
Study Documentation: Experience authoring or reviewing documents such as:
- Data Quality Management Plan (DQMP)
- Data Validation Plan (DVP)
- Data Review Plan (DRP)
- Protocol Deviation Review Plan (PDRP)
- eCRF Completion Guidelines
- Other study-specific Clinical Data Management documentation
Candidates should also have knowledge of the clinical drug-development lifecycle, ICH-GCP, FDA requirements, clinical data standards, SOPs and regulatory submission expectations.
Skills Required
Important skills for this Senior Clinical Data Analyst position include Medidata RAVE, Oracle Clinical, EDC database build, clinical data review, data cleaning, query management, eCRF design, edit checks, UAT, database lock, vendor oversight, eTMF documentation, data quality management, clinical study metrics and stakeholder management.
Strong project management, communication, leadership and mentoring capabilities are also important because the position involves coordination across study teams and guidance to junior Clinical Data Management professionals.
Why Consider This Opportunity?
The Parexel Senior Clinical Data Analyst vacancy provides experienced Clinical Data Management professionals an opportunity to work across the complete clinical study data lifecycle.
The position offers exposure to database build and validation, complex clinical data review, vendor oversight, quality management, study documentation, database lock and cross-functional clinical development activities. It can be particularly relevant for professionals seeking to strengthen their experience in senior-level Clinical Data Management and study leadership responsibilities.
Actual employee benefits, compensation, insurance, leave and other employment benefits should be confirmed directly with Parexel during the recruitment process.
Salary
The official job description does not specify compensation. Based on the seniority and experience requirements of comparable Clinical Data Management positions in India, an indicative salary range of ₹12,00,000–₹22,00,000 per year may be reasonable.
Important: This is an editorial estimate and not a salary range published or guaranteed by Parexel. Actual compensation can vary based on experience, skills, current compensation and company policy.
How to Apply
