Precision Medicine Group is a leading clinical research and biotechnology organization dedicated to advancing personalized medicine. With a strong commitment to data quality and regulatory compliance, the company supports innovative clinical trials worldwide.
Key Responsibilities
As a Central Monitor II, you will:
✔ Conduct risk assessments for clinical studies and develop mitigation strategies.
✔ Perform centralized statistical monitoring to detect data anomalies and trends.
✔ Lead RBQM (Risk-Based Quality Management) initiatives and monthly meetings.
✔ Ensure data quality and integrity through proactive monitoring.
✔ Collaborate with clinical operations, data management, and biostatistics teams.
✔ Prepare detailed reports on monitoring findings for sponsors and study teams.
✔ Track operational metrics (e.g., data entry trends, SDV backlog, site performance).
Qualifications & Skills Required
✅ Education: Bachelor’s degree in Life Sciences, Statistics, Data Management, or related field.
✅ Experience: Minimum 2 years in clinical monitoring, trial management, or equivalent.
✅ Knowledge: Strong understanding of ICH GCP guidelines and RBQM principles.
✅ Technical Skills: Proficiency in statistical analysis tools and data monitoring software.
✅ Soft Skills: Excellent communication, organizational, and problem-solving abilities.
Preferred Qualifications
- Experience working in a CRO (Contract Research Organization).
- Prior exposure to centralized monitoring in clinical trials.
Why Join Precision Medicine Group?
- Work in a dynamic, data-driven clinical research environment.
- Opportunity to mentor junior colleagues and contribute to process improvements.
- Be part of a globally recognized organization in precision medicine.
How to Apply
