BSc Life Sciences Jobs at Precision for Medicine, Apply Online
Looking to take your clinical research career to the next level? Precision for Medicine in Bengaluru is hiring a Central Monitor II to lead centralized monitoring, data integrity, and risk-based quality management (RBQM) for cutting-edge clinical trials. If you have experience in clinical trial oversight, data analytics, and statistical monitoring, this role offers a dynamic and impactful opportunity in a global CRO environment.
About Precision For Medicine
Precision For Medicine is focused on supporting pharmaceutical and life sciences companies in executing successful clinical trials and accelerating drug development. We are dedicated to maintaining the highest standards of data quality, integrity, and risk management throughout the clinical trial process.
Position Summary
The Central Monitor II at Precision For Medicine will be responsible for ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. Key responsibilities include conducting study risk assessments, centralized statistical monitoring, facilitating RBQM meetings, and collaborating across various departments for effective oversight and management of clinical studies.
Key Responsibilities for Central Monitor II Job:
- Study Risk Assessment: Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies, in consultation with functional team leads and PM
- Centralized Statistical Monitoring: Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
- RBQM Meetings: support monthly RBQM meetings by supporting review of study data, documenting findings, action plans and coordination of data cleaning activities to support study deliverables for Central Monitor II.
- Data Quality Assurance: Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
- Collaboration: Work closely with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies
- Reporting: Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
- Operational Insights: Oversee operational study metrics, including data entry trends, SDV backlog, site health trending and proactively communicate issues to study team members to drive towards resolution & proactive remediation
Minimum Required:
- Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical operations) or relevant/equivalent combination of education, training, and experience
- Minimum 2 years experience in clinical monitoring, clinical trial management or equivalent as Central Monitor II
- Working knowledge of ICH GCP guidelines and the clinical development process
Skills:
- Statistical analysis and data monitoring
- Risk assessment and mitigation
- Report writing and presentation
- Collaboration and teamwork
Preferred:
- CRO experience as a Central Monitor
Keywords: Central Monitor II, Precision For Medicine, Clinical Trial Data, RBQM, Statistical Monitoring, Risk Assessment. BSc Life Sciences Jobs at Precision for Medicine, Apply Online
