Clinical Project Start-Up Specialist | fully remote

Praha
Trvalý pracovní poměr
Plný úvazek

Před 3 dny
Snadno podejte žádost

Popis pozice We are currently looking for an experienced Regulatory & Site Start-Up Manager to join an international clinical research project focused on the German market.This is a great opportunity to work on a large-scale study, be part of an experienced global team, and take ownership of key site start-up activities from day one.Your responsibilities:

Lead site start-up activities for clinical trials in Germany
Prepare and submit regulatory documents (including ethics submissions)
Handle ICF adaptation and approvals
Negotiate site contracts and budgets
Support site identification and feasibility
Ensure timely site activation and maintain study timelines
Track progress and maintain SSU documentation and systems
Collaborate with cross-functional teams and provide local regulatory expertise
Ensure compliance with GCP and clinical research regulations

Požadavky

Experience in Site Start-Up (SSU) and site management
Strong background in German regulatory submissions
Hands-on experience with contract and budget negotiations
Fluency in German (C1+) and English (B2+)
Ability to work independently and manage multiple priorities
Strong communication and stakeholder management skills

💡 Nice to have:

Background in clinical research / life sciences

Benefity

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

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