Precision Medicine Group is inviting applications for the Central Monitor II position in Bangalore, Karnataka. This is an excellent opportunity for professionals with experience in clinical monitoring, clinical trial management, Risk-Based Quality Management (RBQM), centralized monitoring, and clinical data review.
If you have experience in clinical operations, centralized statistical monitoring, data quality management, risk assessment, and ICH-GCP, this opportunity offers the chance to work on global clinical trials while collaborating with cross-functional teams in a leading CRO environment.
Job Details
| Category | Details |
|---|---|
| Position | Central Monitor II |
| Company | Precision Medicine Group |
| Location | Bangalore, Karnataka, India |
| Job Type | Full-Time |
| Experience | Minimum 2 Years |
| Qualification | Bachelor’s Degree in Life Sciences, Statistics, Clinical Operations, Data Management or related field |
| Industry | Clinical Research / CRO |
Key Responsibilities
The selected candidate will be responsible for:
- Conduct study-level risk assessments for clinical trials.
- Develop and implement Risk-Based Quality Management (RBQM) plans.
- Perform centralized statistical monitoring to identify trends, anomalies, and risks.
- Review clinical trial data remotely to improve data quality and compliance.
- Support monthly RBQM meetings by documenting findings and action plans.
- Coordinate proactive data cleaning activities.
- Collaborate with Clinical Operations, Data Management, Biostatistics, and Project Management teams.
- Monitor operational metrics including:
- Data entry trends
- SDV backlog
- Site health metrics
- Study performance indicators
- Prepare monitoring reports and sponsor presentations.
- Escalate critical issues and recommend mitigation strategies.
- Mentor junior team members where required.
Required Qualifications
Applicants should possess:
- Bachelor’s Degree in:
- Life Sciences
- Statistics
- Clinical Operations
- Data Management
- Or an equivalent qualification
- Minimum 2 years of experience in:
- Clinical Monitoring
- Clinical Trial Management
- Clinical Research
- Working knowledge of:
- ICH-GCP Guidelines
- Clinical Development Process
- Risk-Based Monitoring
Preferred Skills
Ideal candidates should have experience with:
- Risk-Based Quality Management (RBQM)
- Centralized Monitoring
- Clinical Data Review
- Statistical Data Analysis
- Risk Assessment
- Data Monitoring Dashboards
- Clinical Trial Metrics
- Clinical Systems
- Report Writing
- Data Quality Assurance
- Cross-functional Collaboration
- Scientific Documentation
- Excellent English Communication
Candidates with prior CRO experience as a Central Monitor will have an added advantage.
Why Join Precision Medicine Group?
Working with Precision Medicine Group offers:
- Opportunity to work on global clinical trials
- Exposure to advanced RBQM methodologies
- Collaborative work environment
- Career growth in clinical research
- Experience with centralized statistical monitoring
- Learning opportunities across multiple therapeutic areas
- International quality standards and best practices
Who Should Apply?
This role is ideal for professionals working as:
- Clinical Research Associate (CRA)
- Central Monitor
- Clinical Trial Associate
- Clinical Trial Manager
- Clinical Operations Executive
- Clinical Data Review Specialist
- Risk-Based Monitoring Professional
- Clinical Data Manager
How to Apply
