Location: Bangalore

(Candidates willing to relocate to Bangalore can also apply)

Experience: 4+ Years (End-to-End Clinical Data Management)

How to Apply

Interested candidates with relevant experience in Study Start-Up /

Conduct / Close-Out phases are invited to:

Share your updated CV at: [email protected]
Or refer suitable candidates within your network

Qualified applicants will be reviewed and contacted promptly for the interview process.

Job Summary

We are seeking a Senior Clinical Data Associate II (Sr. CDA II) with robust expertise in Clinical Data Management (CDM) and hands-on experience with EDC tools such as Medidata Rave or Veeva.

The role involves ensuring high-quality clinical trial data through data cleaning, query management, and adherence to GCP and SOP standards.

Key Responsibilities

- Perform data cleaning and discrepancy management activities
- Generate, track, and resolve data queries in EDC systems




- Review clinical data listings for accuracy and consistency
- Analyze data validation checks and reports
- Conduct SAE and vendor reconciliation
- Support CRF design activities (where applicable)
- Prepare project status reports for internal and client stakeholders
- Ensure strict compliance with GCP, SOPs, and study protocols

Mandatory Skills

- 4+ years of experience in End-to-End Clinical Data Management (CDM)
- Hands-on expertise with Medidata Rave or Veeva (mandatory)
- Strong understanding of clinical trial processes and medical terminology
- Experience in query management and data validation
- Good knowledge of GCP guidelines

Education

- Graduate/Postgraduate in Life Sciences
(BSc / MSc / B.Pharm / M.Pharm / Biotechnology or related fields)

Regards,

Gopala BR

Recruitment Lead

📌 Urgent Opening For Sr. CDM For Bangalore (Sr. Clinical Data Mgmt) (Bengaluru)
🏢 Allegis Global Solutions (AGS)
📍 Bengaluru