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Clinical Data Associate

0-2 years
Not Disclosed
10 Nov. 18, 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

Job Title: Clinical Data Associate

Location: Bangalore, India (Office-Based)

Department: Data Management

Experience Required: Minimum 2 years in clinical research, data management, or pharmaceutical industry

About the Role:
Novotech, a global full-service Clinical Contract Research Organization (CRO), is seeking a Clinical Data Associate to join its Data Management team in Bangalore. This role is ideal for professionals with a background in nursing, life sciences, or related fields who are passionate about clinical research and data quality.

As a Clinical Data Associate, you will support day-to-day operations of clinical data management projects, ensuring accurate data acquisition, validation, and reconciliation while maintaining compliance with ICH-GCP, internal SOPs, and regulatory requirements.

Key Responsibilities:

  • Perform data entry and validation using Clinical Data Management software.

  • Assist in generating and resolving data queries with sponsors and monitoring teams.

  • Track CRF pages received, data queries, and database updates.

  • Support Clinical Data Managers (CDMs) in database testing, edit checks, and data cleaning.

  • Collaborate with CDMs to generate reports, listings, and other study outputs.

  • Coordinate coding activities, electronic data transfers, and resolve discrepancies.

  • Maintain systems to track study progress, including CRF & query flow, safety reports, and other data management tools.

  • Participate in project meetings and assist with agenda/minute preparation.

  • Contribute to process improvement initiatives and ensure adherence to quality policies.

  • Support the professional image of Novotech in all external communications.

  • Engage in professional development activities, including conferences and industry forums.

  • Perform other tasks as delegated by the Line Manager to support the Data Management team.

Qualifications & Skills:

  • Graduate in nursing, life sciences, or related field; relevant allied qualifications considered.

  • Minimum 2 years’ experience in clinical research, pharmaceutical industry, or clinical data management.

  • Knowledge of clinical trial processes and data management principles.

  • Strong attention to detail, analytical skills, and problem-solving ability.

  • Excellent communication, teamwork, and multitasking skills.

  • Ability to work in a fast-paced, collaborative, and global environment.

Why Join Novotech:

  • Work in an inclusive, supportive, and flexible workplace committed to gender equality and diversity.

  • Opportunities for professional development within a global CRO spanning Asia-Pacific, North America, and Europe.

  • Exposure to advanced therapeutic areas and regulatory expertise in clinical trials.

  • Participate in meaningful projects that accelerate the development of life-changing medical treatments.

  • Access to wellness programs, flexible leave policies, and career growth opportunities.

About Novotech:
Novotech is a leading global CRO headquartered in Sydney, Australia, with 34 offices worldwide and more than 3,000 employees. The company provides end-to-end clinical development services across all phases of clinical trials, including feasibility assessments, regulatory submissions, data management, statistical analysis, safety solutions, central lab services, and project/vendor management. Novotech is ISO 27001 and ISO 9001 certified, reflecting the highest standards of information security and quality management.

How to Apply:
Submit your resume to join a dynamic team advancing clinical research and contributing to patient safety worldwide.

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