Central Monitoring Manager

atPSI CRO AGRemoteLV flagLatviaFull-timeManagerMid-levelSenior

Posted Sep 8

This is a fully remote position, open to applicants in Latvia.

📋 Description

• Lead and oversee both the initial and ongoing Risk Management for studies.

• Engage in the selection and implementation of the risk-based monitoring platform.

• Conduct Centralized Monitoring, which includes analyzing Key Risk Indicators, performing Statistical Analyses, and establishing Quality Tolerance Limits.

• Deliver Centralized Monitoring analysis findings to study teams and clients.

• Address issues within a collaborative, cross-functional environment.

• Create and evaluate study-specific plans.

• Establish and oversee targeted Source Data Verification (SDV) and monitoring strategies.

• Organize and manage Central Data Review activities.

• Contribute to proposals and participate in bid defense meetings, sharing insights about Risk Based Monitoring services.

• Convey study-related challenges to the Clinical Data Science group and devise data-driven solutions.


⛳️ Requirements

• A college or university degree, or an equivalent combination of education, training, and experience.

• Experience as a Clinical Study Lead or Manager.

• Excellent communication and presentation abilities.

• Strong leadership skills and the capability to work independently.

• Proficient in critical thinking and analytical skills.

• Ability to navigate complex data and derive insights from risk reports and trends.

• Flexibility to adapt to evolving circumstances and a quick learning capacity.

• Understanding of clinical trial processes and functions.

• Capability to comprehend protocols and associated study risks.

• Full working proficiency in English; proficiency in Latvian is a plus.

• Skilled in MS Office applications, particularly Excel.


🏝️ Benefits

• Employees have the option to work remotely.

• Experience stability and innovation at a prominent Contract Research Organization.

• Opportunity to be at the forefront of the clinical research industry.

• Chance to develop risk-based models and gain a comprehensive view of each project.

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