Ref #: 25877

Employment type: Permanent - Full-Time

Location: Santiago, Chile

Posted: 18-Dec-2020

Description

Knowledge of the life cycle management of Investigational Medicinal Products (IMP) and non-IMP from receipt to destruction.
Experience with IVRS, IMP and non-IMP inventory tracking including usage, returns, reconciliation and destruction is desirable.
Basic knowledge of Good Clinical Practices (GCP), Good Manufacturing Practices (GMP), CFR, ICH regulations pertaining to IP desirable.
Computer experience with Microsoft Office (especially Excel), IMPACT (or any clinical trial management system) and Interactive Voice Response System (IVRS) valuable.
Must have excellent verbal and written communication skills able to work with a diverse group of customers, including international.
Attention to detail is critical.

Bachelor degree and 6-8 years experience in clinical operations within the pharmaceutical industry with 3-5 years clinical monitoring.