KCR
Clinical Monitoring • Functional Service Provider • Site Set up and Contracting • Late Phase • Medical & Regulatory Affairs
Senior Specialist II - Site Resourcing
December 13
KCR
Clinical Monitoring • Functional Service Provider • Site Set up and Contracting • Late Phase • Medical & Regulatory Affairs
Description
• Supervision over the completeness of the Study documentation • Supplementing and updating of the Study’s documentation • Cooperation with external suppliers • Coordination of the Center's work as part of the Study • First contact for the CRA • Support for CRA during monitoring visits • Participation in audits • Arranging Patient visits • Active screening for potential Patients • Other activities as instructed by the Investigator.
Requirements
• At least 1 year of experience • University degree in medicine, biotechnology, pharmacy, nursing or biology • Knowledge of English • Very good understanding of ICH-GCP guidelines • Previous experience in clinical trials would be a strong asset • Availability to work at the clinical research site • Strong organizational, communication and teamwork skills • Computer literacy • Mobility • Time flexibility.
Benefits
• High class professional working equipment • Onboarding process to enable you fast takeover of duties • International and supportive environment • Friendly working atmosphere.
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