Clinical Study Administrator - Contracts And Budgets
Vacancyz
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Ich-gcp and local regulations knowledge
Electronic trial master file (etmf) maintenance
Contract negotiation and payment processing
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The Clinical Study Administrator position at Vacancyz involves coordinating and administering clinical studies, managing documentation, and ensuring compliance with regulatory requirements. The role requires strong communication and organizational skills, as well as knowledge of drug development processes and international guidelines.
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Job Summary
The role involves coordinating clinical studies from start-up through execution and close-out while serving as the main local administrative contact.
Candidates will manage document submissions to Ethics Committees and maintain inspection-ready electronic Trial Master Files in compliance with ICH-GCP.
This position requires acting as a primary point of contact for legal negotiations regarding confidentiality agreements and processing payments to healthcare organizations.
Matching Summary
Match Score: 75
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The Clinical Study Administrator position at Vacancyz involves coordinating and administering clinical studies, managing documentation, and ensuring compliance with regulatory requirements. The role requires strong communication and organizational skills, as well as knowledge of drug development processes and international guidelines.
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Skills & Requirements
Must-have
ICH-GCP and local regulations knowledge
Electronic Trial Master File (eTMF) maintenance
Contract negotiation and payment processing
AstraZeneca tracking tools proficiency
Ethics Committee submission support
Nice-to-have
Strong self-accountability and learning agility
Effective stakeholder engagement skills
Cultural awareness in virtual settings
Risk-based thinking and problem solving
Ability to optimize cost and time delivery
Key Requirements
Bachelor's degree aligned with role requirements
Relevant knowledge of drug development process
Fluency in written and spoken business-level English