Urgent Opening For Sr. Cdm For Bangalore (sr. Clinical Data Mgmt) @ LifeScience Clinical

Job Description

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 strong 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

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Keyskills:   Clinical Cdm Study Startup Clinical Data Management CDM Analyst Clinical Data Analyst Veeva study close out Life Sciences Rave Clinical Data Startup Clinical Data Specialist