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.
#Hiring #ClinicalDataManagement #DataAssociate #PharmaJobs #CROJobs #Novotech
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