31 jul
|
Worldwide Clinical Trials d.o.o.
|
Santa Fe
31 jul
Worldwide Clinical Trials d.o.o.
Santa Fe
Worldwide Clinical Trials d.o.o. is seeking a Records Management Compliance professional to manage TMF processes in a integral context. You will handle document processing, reviews, and quality control to ensure regulatory compliance and high data integrity across trials.
Requirements include a university degree (life sciences preferred) and up to 1–2 years in TMF within CRO/pharma. Strong attention to detail and proficiency with Word/Excel are essential.
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📌 Remote TMF Operations Associate II — Impact & Growth (Santa Fe)
🏢 Worldwide Clinical Trials d.o.o.
📍 Santa Fe