Clinical Data Management - Associate - GO/JC/4905/2026

Golden Opportunities; Mumbai; Hybrid; INR 900,000 - 1,300,000; Full time

Job summary

Golden Opportunities in Mumbai is seeking a Clinical Data Management professional to oversee data from collection to database lock, ensuring accuracy and regulatory compliance.

You will review, clean, validate, and reconcile data, develop CRFs/eCRFs, and coordinate with Clinical Operations and Biostatistics to ensure data quality. 1.5 to 10 years of pharma experience is expected with Life Science education and exposure to EDC systems like Medidata Rave, Inform, and Veeva.

Qualifications

• Knowledge of clinical trials and the clinical data management lifecycle.
• Strong analytical, communication, documentation, and problem-solving skills.
• Experience with EDC systems such as Medidata Rave, Inform, Veeva is advantageous.
• Quality-driven data handling from collection to database lock.
• Ability to coordinate with cross-functional study teams.

Responsibilities

• Manage clinical trial data from collection through database lock.
• Review, clean, validate, and reconcile clinical study data.
• Coordinate with Clinical Operations, Biostatistics, Medical Coding, Safety, and other study teams.

Skills

Clinical trial knowledge

Analytical skills

Communication

Documentation

Problem solving

Education

Any Life Science Graduate

Tools

Medidata Rave

Inform

Veeva

Job description

Job Details

Job Title: Clinical Data Management

Job Location: Mumbai, Pune, Hyderabad, Bangalore, Kolkata

Work Model: Hybrid

Candidate Expectations

Total and Relevant Experience – 1.5 Years to 10 Years

Candidate Location - Anywhere

Skills – Startup, Conduct, Closeout

Candidate Industry (Pharma)

Diversity – No

Education and Certification

Qualification: Any Life Science Graduate

Specific Remarks: Distance education not accepted.

Certification: Not Applicable

Detailed Job Description

• Manage clinical trial data from collection through database lock.
• Review, clean, validate, and reconcile clinical study data.
• Develop and review CRFs/eCRFs, edit checks, data validation specifications, and data management plans.
• Perform data review, query generation, tracking, and resolution.
• Coordinate with Clinical Operations, Biostatistics, Medical Coding, Safety, and other study teams.
• Perform data reconciliation across EDC, labs, safety, and other external data sources.
• Support database testing, UAT, and database lock activities.
• Maintain clinical data management documentation in accordance with SOPs, GCP, and applicable regulations.
• Identify data issues and support process improvements.

Key Skills

Knowledge of clinical trials and the clinical data management lifecycle.

Experience with EDC systems such as Medidata Rave, Inform, Veeva is advantageous.

Knowledge of medical coding and data reconciliation is a plus.

Strong analytical, communication, documentation, and problem-solving skills.

Mandatory Skills

Set up - Edit check , UAT, EDC, Protocol review

Conduct - Query Management , External Data Reconciliation, Data Validation and Cleaning

Close out: Database Lock

Additional Requirements

Proper documents for entire career and PF Form 16 Mandatory