Monitoring Manager

🔥 3 minutes ago

🇱🇹 Lithuania – Remote

💵 €77k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 0%

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Lead and facilitate initial and ongoing study Risk Management • Participate in selection and setup of the RBM platform • Perform Centralized Monitoring for a study, including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits • Present Centralized Monitoring analysis results to study teams and clients • Manage issues in a cross-functional environment • Develop and review study-specific Plans • Set up and manage targeted SDV and monitoring strategy for a study • Set up and manage Central Data Review activities in a study • Contribute to Proposals and bid defense meetings with information about Risk Based Monitoring services • Communicate study challenges to the Clinical Data Science group and develop data-driven solutions

🎯 Requirements

• College/University degree or an equivalent combination of education, training and experience • Clinical Study Lead/Manager experience • Strong communication and presentation skills • Leadership and ability to work independently • Critical thinking and analytical skills • Ability to work with complex data and provide insight into risk reports and trends • Ability to adapt to changing circumstances and learn quickly • Knowledge of the process and functions in clinical trials • Ability to understand the protocol and study-associated risks • Full working proficiency in English; Lithuanian proficiency is a plus • Proficiency in MS Office applications • Excel skills

🏖️ Benefits

• Excellent working conditions • Extensive training • Friendly team • Opportunities for personal and professional growth • Fair and attractive salary and benefits package