Job Overview
Location
Bangalore, Karnataka, India
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • The Central Monitor II plays a key role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management, directly supporting the reliability of clinical research outcomes.
- • Day-to-day responsibilities include conducting study risk assessments, performing centralized statistical monitoring and data analysis to detect anomalies, supporting monthly RBQM meetings, preparing detailed reports and presentations, overseeing operational study metrics, and collaborating with clinical operations, data management, and biostatistics teams to ensure data quality and compliance.
- • Precision Medicine Group is a leader in precision medicine solutions, providing integrated services across clinical development, data analytics, and commercialization, with a commitment to improving patient outcomes through innovative research and rigorous quality standards.
- • In this role, the individual will develop expertise in Risk-Based Quality Management (RBQM), gain hands-on experience with centralized statistical monitoring, strengthen leadership and mentoring capabilities, and contribute to process improvements that enhance team efficiency and data integrity across complex clinical studies.
🎯 Requirements
- • Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical operations) or equivalent combination of education, training, and experience
- • Minimum 2 years experience in clinical monitoring, clinical trial management, or equivalent
- • Working knowledge of ICH GCP guidelines and the clinical development process
- • Strong understanding of RBQM principles and methodologies
- • Proficiency in statistical analysis and data monitoring tools
- • Excellent organizational and time management skills
🏖️ Benefits
- • Opportunity to mentor junior colleagues and support team development
- • Involvement in developing processes, procedures, and documentation to ensure high team functioning
- • Exposure to complex studies and portfolios, enabling professional growth in centralized monitoring
- • Collaboration with cross-functional teams including clinical operations, data management, and biostatistics
- • Role based in Bangalore, Karnataka, India, within a global organization committed to equal opportunity employment
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
Subscribe to the weekly newsletter for similar remote roles and curated hiring updates.
Newsletter
Weekly remote jobs and featured talent.
No spam. Only curated remote roles and product updates. You can unsubscribe anytime.
Similar Opportunities
Integer Holdings Corporation
2 months ago