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Data Process Associate

0-2 years
Not Disclosed
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Data Process Associate

Job ID: ATR2114
Location: Bengaluru, Karnataka, India
Job Type: Full-time (On-site)
Department: Data Management


Overview

Join Quanticate, a leading data-focused CRO, as a Data Process Associate and play a key role in ensuring accurate and compliant clinical data management. This position offers hands-on experience, skill development, and the opportunity to contribute to impactful clinical trials that advance global healthcare outcomes.


Key Responsibilities

  • Accurately enter and verify clinical trial data from Case Report Forms (CRFs) into study databases following established guidelines.

  • Perform quality control checks to ensure data accuracy, integrity, and compliance with regulatory standards.

  • Assist in database testing, documentation preparation, and data processing across multiple projects.

  • Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation.

  • Collaborate with project managers and cross-functional teams to meet project timelines.

  • Identify and recommend process improvements to enhance efficiency and data quality.

  • Perform medical coding activities and other tasks as assigned to support study completion.


What You Will Gain

  • Practical experience in clinical data management within a regulated environment.

  • Knowledge of ICH guidelines, GCP, and industry data handling regulations.

  • Exposure to global, cross-functional clinical research teams and project management practices.

  • Development of strong analytical, technical, and communication skills using industry-leading tools.

  • A foundation for long-term career growth in data management and clinical research.

  • The opportunity to contribute to clinical studies that improve healthcare and patient outcomes.


Education & Qualifications

  • Master’s degree in Life Sciences or related field.


Skills & Experience

  • Proficiency with PC applications (Excel, Word).

  • Basic knowledge of Clinical Data Management processes.

  • Understanding of ICH Guidelines and GCP principles, especially regarding data handling.

  • Strong analytical skills and attention to detail.

  • Effective oral and written communication skills.

  • Ability to manage competing priorities in a dynamic environment.

  • Team-oriented mindset with the ability to inspire collaboration and motivation.


Benefits

  • Competitive salary package.

  • Six-month intensive training plan for skill development.

  • Flexible working hours.

  • Paid leave: annual leave, sick leave, casual leave, and bank holidays.

  • Medical insurance for self and immediate family.

  • Gratuity and accidental coverage.

  • Access to career development opportunities including mentoring, coaching, e-learning, and job shadowing.


About Quanticate

Quanticate is a world-leading data-focused CRO, providing advanced clinical data management, statistical programming, and biostatistics solutions. We partner with top pharmaceutical companies and biotech startups, offering opportunities to contribute to world-class clinical programs. We strongly advocate career development, professional society memberships, and continuous learning to help you build a rewarding career in clinical research.


⚠️ Note: Quanticate will never request payments during the hiring process. All legitimate communication will come from an @quanticate.com email domain.