Regulatory & Site Start-Up Manager | fully remote

We are looking for a proactive and organized professional to support our client with clinical projects and help manage documentation for clinical sites.

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

Start date: immediately

Contract for limited period with possibility of prolongation

NABÍZÍME

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

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

DALŠÍ POŽADAVKY

• angličtina (C1 - aktivně)
• němčina (C1 - aktivně)

Send us your CV in English and Czech if you have one. For more related job opportunities visit https://www.grafton.cz/en/job-search

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