Senior Data Scientist / ML Engineer
AmbushBuild forecasting, optimization, and AI solutions at Ambush, an engineering and strategy consultancy. Develop secure Python services and take machine learning systems into production.
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IQVIA combines healthcare data analytics, advanced technology, and consulting to help organizations address complex challenges across the life sciences and healthcare sectors. Its Connected Intelligence platform brings together data and artificial intelligence to support clinical research, technology development, and the advancement of new therapies. The company’s teams work across analytics, consulting, and healthcare technology, offering opportunities connected to research, digital innovation, and efforts to improve patient outcomes.
Local Clinical Study Manager, Eastern Europe (Remote)
Lead oncology and onco-hematology clinical trials across Eastern Europe for IQVIA. Oversee clinical teams, site activation, monitoring, regulatory delivery, and study execution.
Description
- Direct daily monitoring activities for complex clinical studies
- Share study objectives, expectations, and progress updates with clinical teams
- Own country-level study commitments and ensure timely, high-quality data delivery
- Provide oversight and leadership for clinical deliverables
- Manage clinical teams and applicable local and global staff
- Lead the successful activation of trial sites
- Monitor the quality of clinical activities and resolve quality concerns
- Review and approve site visit reports while tracking, following up on, and resolving site issues
- Assess data-related risks and issues and create contingency and mitigation plans
- Develop and maintain study-specific plans, documentation, and tools
- Assist CRAs with site monitoring and help resolve site-level challenges
- Supervise regulatory and internal clinical staff to ensure updates, reports, renewals, and end-of-study notifications meet protocols, local regulations, ICH GCP, and applicable procedures
- Coordinate training, process activities, system-related work, and ad hoc tasks
Requirements
- Bachelor’s degree in a related field, preferably life sciences
- At least five years of clinical research experience, including two or more years in project management, or an equivalent combination of education and experience sufficient to perform the role successfully
- Working knowledge of ICH GCP international guidelines and applicable local regulations
- Demonstrated ability to lead and motivate cross-functional teams to deliver clinical trials on or ahead of schedule, within budget, and to the required quality standards
- Professional experience in oncology or onco-hematology is required
- Solid understanding of the drug development process
- Excellent spoken and written English
- Ability to learn and adapt to clinical IT systems
- Sound decision-making skills
- Experience monitoring study activities for compliance and inspection readiness
- Strong interpersonal skills for working with internal teams, stakeholders, and external vendors
- Thorough understanding of clinical operations, including trial data collection and management
Benefits
- Full-time, home-based work arrangement
- Opportunity to manage clinical research projects across multiple therapeutic areas
- Close collaboration with a key client
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