03 ago
|
Worldwide Clinical Trials d.o.o.
|
Neuquén
03 ago
Worldwide Clinical Trials d.o.o.
Neuquén
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 (Neuquén)
🏢 Worldwide Clinical Trials d.o.o.
📍 Neuquén