Regulatory & Site Start-Up Manager | fully remote

Grafton Zobrazit všechny práce

  • Praha
  • Trvalý pracovní poměr
  • Plný úvazek
  • Před 21 dny
  • Snadno podejte žádost
Popis pozice 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 prolongationPožadavky
  • 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
Benefity
  • 5 weeks of paid holiday
  • Possibility to work anywhere from Czech Republic
  • Meal vouchers
  • Cafeteria
  • Mutlisport card
  • Contribution to pension insurance
  • Transport allowance

GigaPráce

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