Associate Regulatory and Start Up Manager - Hungary
Employer · IQVIA
Licensing officer
R&D manager
Health services managerFull-timeBudapest
The Regulatory & Site Activation Manager leads the delivery of site activation, regulatory, and maintenance activities for assigned clinical studies and programs. This role ensures projects are delivered on time, within scope, and in compliance with regulatory requirements while providing leadership, strategic oversight, and support to study teams and clients.
Tasks
- Lead site activation, maintenance, and regulatory activities for assigned studies.
- Develop and oversee project plans, timelines, budgets, and resources.
- Provide regulatory strategy and guidance to support study start-up and ongoing maintenance.
- Identify risks and regulatory challenges, implementing effective solutions.
- Collaborate with global, regional, and country teams to ensure successful project delivery.
- Support business development activities, including proposals and bid defenses.
- Ensure compliance with quality standards, regulatory requirements, and internal processes.
- Mentor and support team members, driving performance and development.
- Maintain accurate project documentation, systems, and tracking tools.
Conditions & benefits
Career DevelopmentDevelop your career in a collaborative and fast-paced environment at a global leader in clinical research.
Requirements
- Bachelor's Degree in a relevant Life Sciences or Healthcare field.
- Minimum 3 years' clinical research experience, including at least 1 year in a leadership or project management capacity.
- Strong knowledge of clinical research, regulatory requirements, and clinical systems.
- Excellent communication, stakeholder management, and presentation skills.
- Proven ability to manage multiple priorities, lead teams, and work independently.
- Strong organizational skills, attention to detail, and problem-solving abilities.