Clinical Data Associate

Roles & Responsibilities
• Enter clinical trial data accurately using Clinical Data Management (CDM) systems
• Review, track, and assist in resolving data queries in coordination with sponsors and monitoring teams
• Maintain records of CRF receipt, data entry status, and query resolution
• Support database testing, edit checks, and data reconciliation activities
• Assist in medical coding, electronic data transfers, and generation of reports and listings
• Coordinate with lead CDMs and project teams to ensure smooth study execution
• Generate project updates, reports, and documentation as required
• Participate in project meetings and assist in preparing agendas and meeting minutes
• Support study tracking tools and data management systems (CRF flow, query flow, safety reports, Novotrak)
• Contribute to process improvement initiatives and provide general administrative support
• Ensure compliance with SOPs, GCDMP guidelines, ICH-GCP, and company quality standards

Qualification
• Graduate in Clinical Sciences, Life Sciences, Pharmacy, or allied disciplines

Experience
• Freshers can apply
• 6 months to 1 year of experience in clinical data management or clinical research is preferred

Skills
• Basic knowledge of clinical data management and CDM software
• Strong attention to detail and data accuracy
• Good communication and teamwork skills
• Ability to follow SOPs and regulatory guidelines

About the Organization
Novotech is a leading global CRO providing full-service clinical development solutions, supporting innovative clinical trials across multiple therapeutic areas while fostering an inclusive and growth-oriented work culture.