Vanda Pharmaceuticals
Berlin, NH, USA
Primary Responsibilities:
You will contribute to the selection of CRO’s and/or potential investigators, train, support and advise investigators and site staff in study-related matters and ensure that study sites are always inspection ready. You will also be responsible for monitoring of CROs in the preparation, initiation, monitoring and closure of assigned sites in clinical studies, ensuring compliance with VANDA’s Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations of study sites.
Education & Experience Requirements:
Undergraduate degree (Bachelor or higher) in Biology, Pharmacy, Medicine, Health Sciences or related field, with a strong academic record
Exposure to basic sciences/clinical research.
Willingness to learn a basic understanding of the drug development process, and ability to adapt within a dynamic environment.
Excellent oral and written communication skills in English and German
Ability to travel...