Central Monitor (India/China)
Location: Bangalore, India – Ground Floor, Unit 1, Block E, Helios Business Park, 560103
Job ID: 3421
Schedule: Full-time
Posting Date: 19 September 2025
Apply Before: 14 October 2025, 06:30 PM
Company Overview
Novotech is a global full-service Clinical Contract Research Organization (CRO):
Headquartered in Sydney, Australia, with 34 offices across Asia-Pacific, North America, and Europe.
Employs over 3,000 employees and partners with 5,000+ clinical sites.
Offers services across all clinical trial phases and therapeutic areas, including:
Feasibility assessments
Ethics and regulatory submissions
Data management & statistical analysis
Medical monitoring & safety solutions
Central lab services
Report writing to ICH requirements
Project & vendor management
Certified with ISO 27001 (Information Security) and ISO 9001 (Quality Management).
Role Overview
The Central Monitor is responsible for risk-based clinical trial monitoring using patient data and site/country/project-level information. The role focuses resources on critical risks impacting data quality and patient safety and involves centralized, remote, and on-site monitoring activities.
Minimum Qualifications & Experience
Education: Bachelor’s degree in Clinical, Life Sciences, Mathematics, Statistics, or related field.
Experience: Minimum 3 years in clinical trials or equivalent combination of education, training, and experience.
Skills & Knowledge:
Strong understanding of GCP and clinical trial processes
Risk identification and trend analysis
Data analysis and technical skills in clinical trials
Good interpersonal and communication skills (English – written & oral)
Ability to work independently and as part of a team
Strong problem-solving and multitasking capabilities
Key Responsibilities
Central Monitoring & Risk Management
Plan central monitoring activities per SOPs and GCP guidelines.
Provide input into the Integrated Quality Risk Management Plan (IQRMP).
Support setup and activation of central monitoring systems.
Monitor patient data, site/country/project-level data, and quality metrics centrally.
Identify risks and propose actions for signal and issue management.
Track action items and ensure timely closure with relevant teams.
Communicate significant non-compliance or critical issues to stakeholders.
Support overall efficiency in clinical trial monitoring strategies.
Documentation & Reporting
Document centralized monitoring activities accurately.
Facilitate and attend central monitoring outcome review meetings.
Provide timely reports on findings, risks, and action resolutions to stakeholders.
Stakeholder Collaboration
Work with cross-functional teams to implement centralized monitoring strategies.
Ensure coordination between internal and external stakeholders for risk mitigation.
Team & Culture
Strategic vs. transactional mindset with ability to make proactive decisions.
Collaborative, inclusive culture where all voices are valued.
Support from senior leadership for professional growth.
Work alongside empowered teams committed to clinical trial excellence.
Equal Opportunity Statement
Novotech is an Equal Employment Opportunity Employer, committed to diversity and inclusion. Employment decisions are based on merit, qualifications, and business requirements, without regard to race, religion, gender, age, sexual orientation, disability, or other protected characteristics.
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