Clinical Data Management Associate

Evoke HR; Ahmedabad District; In loco; INR 300.000 - 520.000; Tempo pieno

Descrizione del lavoro

Evoke HR Solutions Pvt. Ltd. is seeking a detail-oriented Clinical Data Management Associate to support the collection, validation, processing, and management of clinical trial data.

The role focuses on maintaining accurate databases, ensuring data quality, and supporting regulatory-compliant study processes. Ideal candidates have a Pharmacy, Life Sciences, or related background. Freshers with interest in clinical research and data management are welcome to apply, with a foundation in EDC

Competenze

• Bachelor's or Master's degree in Pharmacy, Life Sciences, or related fields.
• Freshers with interest in clinical research and data management are encouraged to apply.
• Basic understanding of clinical trials and clinical research processes.
• Knowledge of medical terminology and clinical documentation.

Mansioni

• Collect, review, and manage clinical trial data from various sources.
• Enter and validate clinical study information in electronic data capture (EDC) systems.
• Review CRFs for accuracy and completeness.
• Identify missing, inconsistent, or incorrect data and assist in resolving discrepancies.
• Generate and manage data queries to ensure accurate documentation.
• Maintain clinical databases and ensure data integrity throughout the study lifecycle.
• Support database cleaning, reconciliation, and data validation activities.
• Coordinate with clinical research associates, investigators, and other study teams.

Conoscenze

Clinical data entry

Data validation

CRFs knowledge

Data cleaning

EDC systems

MS Excel

Formazione

B.Pharm / M.Pharm

Pharm.D

Life Sciences

Biotechnology

Microbiology

Descrizione del lavoro

Job Title: Clinical Data Management Associate
Department: Pharmaceutical & Biotechnology
Role: Clinical Research Scientist
Experience: 01 Years (Freshers Can Apply)
Job Type: Full-Time

About the Role

We are seeking a detail-oriented Clinical Data Management Associate to support the collection, validation, processing, and management of clinical trial data. The candidate will be responsible for maintaining accurate clinical research databases, ensuring data quality, identifying discrepancies, and supporting clinical research teams in compliance with regulatory and study requirements.

Key Responsibilities

• Collect, review, and manage clinical trial data from various sources.
• Enter and validate clinical study information in electronic data capture (EDC) systems.
• Review clinical trial records and case report forms (CRFs) for accuracy and completeness.
• Identify missing, inconsistent, or incorrect data and assist in resolving data discrepancies.
• Generate and manage data queries to ensure accurate clinical trial documentation.
• Maintain clinical databases and ensure data integrity throughout the study lifecycle.
• Support database cleaning, reconciliation, and data validation activities.
• Coordinate with clinical research associates, investigators, and other study teams.

Eligibility

• Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm), Pharm.D, Life Sciences, Biotechnology, Microbiology, or related disciplines.
• Freshers with an interest in clinical research and data management are encouraged to apply.
• Basic understanding of clinical trials and clinical research processes.
• Knowledge of medical terminology and clinical documentation.

Required Skills

• Clinical data entry and data validation.
• Clinical trial documentation.
• Knowledge of Case Report Forms (CRFs).
• Data cleaning and query management.
• Basic understanding of Electronic Data Capture (EDC) systems.
• MS Excel and MS Office proficiency.