What you will do:

• Prepare and review regulatory documents for clinical sites
• Assist with site contract and budget negotiations
• Support the team in project planning and tracking progress
• Ensure document quality and compliance with GCP standards
• Provide feedback and support to the project team and management
• Participate in site selection and other project activities as needed

Požadujeme:

• Degree in a scientific or healthcare field preferred, or a combination of education and relevant experience
• Experience with regulatory submissions in Germany
• Hands-on experience with site contract and budget negotiations
• Solid background in Site Start-Up (SSU) activities and site management
• Fluent in English and German
• Strong organizational and problem-solving skills
• Ability to manage multiple priorities and communicate effectively with different stakeholders
• Knowledge of GCP and clinical research regulations is a plus
• počet míst - 1

Nabízíme:

• 5 weeks of paid holiday
• Possibility to work anywhere from Czech Republic
• Meal vouchers
• Cafeteria
• Mutlisport card
• Contribution to pension insurance
• Transport allowance