Ensure performance of assigned reviews with high quality, on-time results with more complex analyses or deeper root cause analyses to connect related signal to risks
Provide training and guidance to junior team members
Independently lead the design and setup of study specific tools and centralized monitoring plan for data review
Manage review timelines, develop analysis assignments for team, and support budget management
Lead report development, deliver reports, and lead centralized monitoring meetings
Contribute to risk assessment through the completion of the department risk assessment tools
Participate in the cross-functional risk assessment review meetings and contribute to overall risk planning

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Comparable to 8+ years’ experience in clinical monitoring, data management, biostatistics, or related field in support of clinical trials is preferred
Strong attention to detail with proficient organization and multi-tasking skills
Excellent analytical/problem-solving skills/judgment in decision making
Ability to lead, motivate and coordinate teams, including coaching/mentoring team members
Demonstrated ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
Strong computer skills, with strong knowledge of MS Office (Word, Excel, PowerPoint)

Reasonable accommodation for individuals with disabilities during application or interview process
Professional development opportunities
Flexible working environment with collaboration and innovation as part of everyday experience

Principal Centralized Monitoring Analyst – Risk Manager

Key skills