Clinical Data Management (CDM) Associate

About the Role

Clinogenesis Research Organization is offering an entry-level opportunity for fresh graduates to build a career in Clinical Data Management (CDM). In this role, you will work alongside clinical data specialists to ensure the accuracy, completeness, and integrity of clinical trial data processed through Electronic Data Capture (EDC) systems.

Key Responsibilities

• Assist in reviewing Case Report Forms (CRFs/eCRFs) for completeness, accuracy, and logic.
• Log, issue, and track data queries to clinical sites to resolve discrepancies.
• Support data entry, verification, and data validation activities according to the Data Management Plan (DMP).
• Participate in database testing, discrepancy management, and data reconciliation checks.
• Maintain clinical data documentation while ensuring compliance with Good Clinical Data Management Practices (GCDMP) and GCP guidelines.

Eligibility Criteria

• Education: B.Pharm, M.Pharm, Pharm.D, B.Sc / M.Sc in Life Sciences, Biotechnology, Microbiology, Bioinformatics, Nursing, or allied health fields.
• Certification: Mandatory certification in Clinical Data Management (CDM) / Clinical Research (with hands-on knowledge of EDC systems, CDISC standards, or query management).
• Experience: Freshers only (2024 / 2025 / 2026 graduates).

Key Skills

• Strong foundational understanding of clinical data workflows, CRF design, and query life cycles.
• Excellent computer skills, including proficiency in MS Excel and database management basics.
• Exceptional attention to detail, analytical mindset, and data precision.

Why Start at Clinogenesis?

• Direct exposure to real-world clinical trial databases and data handling workflows.
• Structured mentorship from experienced clinical data managers.
• A clear career progression path within data management, biostatistics, and clinical operations.