Responsibilities
- Lead and coordinate risk management activities throughout the lifecycle of clinical studies
- Support the evaluation and implementation of risk-based monitoring platforms
- Conduct centralized monitoring tasks, including assessment of key risk indicators, statistical evaluations, and quality tolerance thresholds
- Share findings from centralized monitoring with study teams and clients, addressing issues across functional teams
- Create and evaluate study-specific monitoring and risk management plans
- Design and oversee targeted source data verification and monitoring approaches tailored to study needs
- Establish and supervise central data review processes within clinical studies
- Support business development by providing risk-based monitoring expertise during proposal and bid defense stages
- Collaborate with data science teams to identify study challenges and develop data-informed solutions
Requirements
- Bachelor's degree or equivalent combination of education, training, and relevant experience
- Prior experience in clinical study leadership or management roles
- Excellent communication and presentation abilities
- Proven leadership skills and capacity to work autonomously
- Strong critical thinking and analytical capabilities
- Skilled in interpreting complex data and identifying patterns in risk reports
- Adaptable to dynamic environments with quick learning ability
- Solid understanding of clinical trial processes and protocols, including risk identification
- Fluent in English with full professional working proficiency
- Proficient in MS Office, particularly advanced Excel functions
Nice to Have
- Experience in centralized monitoring is advantageous
- Knowledge of Latvian language is beneficial
Other
Opportunity to work at the forefront of the industry, help shape risk-based monitoring frameworks, and gain a comprehensive, global perspective on project execution
