Central Monitor II

Job Description

Precision Medicine Group is seeking a Central Monitor II to ensure the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. The Central Monitor II works independently and manages report review and issue escalation for more complex studies and/or portfolios of work. Further, the Central Monitor II may mentor junior colleagues, and may support the development of processes, procedures and other documentation to ensure a high functioning team.Role involves:

• Conducting study risk assessments.
• Performing centralized statistical monitoring & data analysis.
• Supporting monthly RBQM meetings.
• Ensuring data quality assurance.
• Preparing detailed reports and presentations.
• Overseeing operational study metrics.

Requirements:

• Bachelor’s Degree in a relevant field.
• Minimum 2 years experience in clinical monitoring or clinical trial management.
• Working knowledge of ICH GCP guidelines.
• Highly effective communication skills.
• Excellent organizational and time management skills.
• Strong understanding of RBQM principles.
• Proficiency in statistical analysis and data monitoring tools.
• Detail-oriented with strong analytical and problem-solving skills.

Role offers:

• Opportunity to play a key role in ensuring the quality and integrity of clinical trial data.
• Chance to work independently and manage report review and issue escalation.
• Opportunity to mentor junior colleagues and support the development of processes and procedures.