Clinical Data Management professionals looking for their next career opportunity can now apply for the CDA II (Clinical Data Associate II) position at Precision For Medicine. This hybrid opportunity is open to candidates currently residing in Bangalore or Chennai with hands-on experience across the complete clinical trial lifecycle.
If you have expertise in Study Setup, CRF Design, UAT, Data Review, Data Reconciliation, SAE Reconciliation, Database Freeze, and Database Lock, this could be an excellent opportunity to advance your career in Clinical Data Management.
Precision For Medicine Hiring CDA II โ Overview
| Details | Information |
|---|---|
| Job Title | CDA II (Clinical Data Associate II) |
| Company | Precision For Medicine |
| Job Location | Bangalore / Chennai |
| Work Mode | Hybrid |
| Department | Clinical Data Management |
| Employment Type | Full-Time |
| Experience | Clinical Data Management Professionals |
| Preferred Therapeutic Area | Oncology |
Clinical Data Associate II Responsibilities
As a Clinical Data Associate II, you will contribute throughout the clinical trial lifecycle by ensuring high-quality clinical data collection and management.
Key responsibilities include:
- Perform study setup activities including CRF review and configuration
- Support Clinical Metadata Testing (CMT)
- Execute User Acceptance Testing (UAT) for EDC systems
- Conduct ongoing clinical data review
- Perform data reconciliation activities
- Manage SAE reconciliation with pharmacovigilance teams
- Support database freeze and database lock activities
- Ensure data quality and compliance throughout clinical trial phases
- Collaborate with cross-functional clinical teams
- Follow ICH-GCP and sponsor SOPs
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline
- Practical experience in Clinical Data Management
- Hands-on exposure to:
- CRF
- CMT
- UAT
- Data Review
- Data Reconciliation
- SAE Reconciliation
- Database Freeze
- Database Lock
- Experience across one or more clinical trial phases
- Strong understanding of clinical trial processes and data quality standards
Preferred Qualification
- Experience in Oncology Clinical Trials is highly preferred.
Skills Required
- Clinical Data Management
- Electronic Data Capture (EDC)
- CRF Development
- UAT Testing
- Clinical Data Review
- SAE Reconciliation
- Database Lock
- Clinical Trial Lifecycle
- Oncology Studies
- ICH-GCP
- Cross-functional Collaboration
- Data Quality Management
Why Join Precision For Medicine?
Working with Precision For Medicine offers professionals an opportunity to:
- Work on global clinical research projects
- Gain experience across the complete clinical trial lifecycle
- Collaborate with experienced Clinical Data Management professionals
- Hybrid working model
- Exposure to oncology clinical studies
- Career growth within an international clinical research organization
Who Can Apply?
Candidates who:
- Are currently based in Bangalore or Chennai
- Have relevant Clinical Data Management experience
- Have worked across study setup, conduct, and closeout activities
- Can support database freeze and database lock processes
- Are passionate about clinical research and data quality
How to Apply
Interested candidates should email their updated resume to:
Email: roopa.ramaiah@precisionformedicine.com
Subject Line Format:
CDA II | Current Notice Period
Example:
CDA II | Immediate Joiner