Senior Clinical Data Analyst
India, Hyderabad
- Pay
- Salary not listed in the saved posting
- Work setup
Hybrid stated — work setup source
Provide training and mentoring to junior Clinical Data Management staff. Location : Office Based (Hybrid)
Read the full posting- Employment
- Unconfirmed
What you’ll work on
Full postingSupport DML in study planning, execution, and project management activities.
Create and maintain study documents and ensure filing in eTMF per study requirements.
Support Data Quality Review meetings and provide study metrics.
From the employer’s posting
Key Responsibilities Support DML in study planning, execution, and project management activities. Draft EDC build timelines and perform database/edit check specification activities.
Conduct UAT/testing for database, coding, site payment, and safety integrations. Create and maintain study documents and ensure filing in eTMF per study requirements. Coordinate data review activities and vendor deliverables.
Coordinate data review activities and vendor deliverables. Support Data Quality Review meetings and provide study metrics. Manage post-production, migration, and database lock activities.
Tools in this posting
- Oracle
Source — Tool mentions in context
- 8+ years of End-to-end Clinical Data Management experience from protocol review, CRF/eCRF design through database lock. - Strong experience in EDC systems: Medidata RAVE and Oracle Clinical. - Expertise in Data Review, Query Management, Query Trend Analysis, Protocol Deviation Review, and Data Quality oversight.
Job description
Job Summary
The Clinical Data Management Associate will support the Data Management Lead (DML) in the planning, setup, execution, monitoring, and closeout of clinical studies. The role is responsible for database build activities, data review, vendor oversight, study documentation, quality management, and ensuring high-quality clinical data delivery in compliance with regulatory requirements, SOPs, and study timelines.
Key Skills & Experience
- 8+ years of End-to-end Clinical Data Management experience from protocol review, CRF/eCRF design through database lock.
- Strong experience in EDC systems: Medidata RAVE and Oracle Clinical.
- Expertise in Data Review, Query Management, Query Trend Analysis, Protocol Deviation Review, and Data Quality oversight.
- Experience authoring and reviewing DQMP, DVP, DRP, PDRP, eCRF Completion Guidelines, and related study documents.
- Knowledge of FDA/ICH-GCP guidelines, clinical drug development process, and regulatory submission requirements.
- Experience overseeing CRO/CDM vendors and managing study deliverables within timelines.
- Strong project management, metrics reporting, and stakeholder management skills.
- Experience supporting audits, inspections, and cross-functional study teams.
- Excellent communication, mentoring, and leadership abilities.
Key Responsibilities
- Support DML in study planning, execution, and project management activities.
- Draft EDC build timelines and perform database/edit check specification activities.
- Conduct UAT/testing for database, coding, site payment, and safety integrations.
- Create and maintain study documents and ensure filing in eTMF per study requirements.
- Coordinate data review activities and vendor deliverables.
- Support Data Quality Review meetings and provide study metrics.
- Manage post-production, migration, and database lock activities.
- Ensure high-quality, timely study delivery in compliance with SOPs and regulatory requirements.
- Provide training and mentoring to junior Clinical Data Management staff.
Location : Office Based (Hybrid)
Your next step
- Have your CV and examples of relevant work ready.
- Check the listed location, eligibility and core experience before starting.
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Source & posting history
Source notes
Source excerptsSelected passages from the saved posting. Check the full description for conditions and exceptions.
- Pay
No pay amount identified in the saved description.
- Location & working pattern
India, Hyderabad
- Provide training and mentoring to junior Clinical Data Management staff. Location : Office Based (Hybrid)
- Work authorization
No clear work-authorization passage found. Eligibility is unconfirmed.
- Status in our records
- Active
- First seen by us
- Aug 13, 2026
- Recorded sightings
- 266
- Last seen by us
- Oct 9, 2026
These dates show when we found the listing. Check the employer’s website to confirm it is still accepting applications.
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