Latest Clinical Operation Jobs at Precision Medicine Group | Apply Now
Are you passionate about clinical research and data-driven healthcare? Precision Medicine Group is hiring for the role of Central Monitor II at its Bengaluru, Karnataka location. This is an exciting opportunity to work with a forward-thinking organization that is redefining patient care through precision medicine. If you have experience in clinical monitoring, risk assessment, and centralized data review, join a team that’s transforming clinical trials through innovation and integrity.
About Precision Medicine Group
Precision Medicine Group is a global, innovation-driven organization dedicated to transforming healthcare by advancing the science of precision medicine. Through a combination of deep scientific knowledge, cutting-edge technology, and data analytics, the company supports life sciences clients in designing, executing, and optimizing targeted therapies. With a commitment to improving patient outcomes, Precision Medicine Group operates with integrity, quality, and a focus on collaboration across clinical development and commercialization.
Job Title: Central Monitor II
Location: Bengaluru, Karnataka, India
About the Job
The Central Monitor II will play a crucial role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development
of Risk-Based Quality Management (RBQM) plans, conducting risk assessment studies, central statistical monitoring, data review, and facilitating RBQM meetings.Qualifications:
- 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 of experience in clinical monitoring, clinical trial management, or equivalent
- Working knowledge of ICH GCP guidelines and the clinical development process
Preferred Skills:
- Highly effective oral and written communication skills, with the ability to communicate effectively with project team members
- Excellent organizational and time management skills
- Excellent written and spoken English, including strong grammar and scientific vocabulary skills
- Ability to work in a team or independently as required
- Strong understanding of RBQM principles and methodologies.
- Demonstrated ability to learn how to extract pertinent information from protocols, electronic study data systems, clinical systems, dashboards, and to leverage these data to assess risk
- Proficiency in statistical analysis and data monitoring tools.
- Detail-oriented with strong analytical and problem-solving skills.
Essential functions of the job include, but are not limited to:
- 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 coordinating data cleaning activities to support study deliverables
- 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
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