Carriere Switch

Deze vacature is ouder dan 40 dagen...

1

sollicitant

Reddingsgeld om snel wat extra geld te bekomen in tijden van nood. Lenen t/m Euro 300,- met een looptijd van 10 tot 28 dagen.

Responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance to Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.

Skills:
• Through understanding of clinical research principles and process
• Good understanding of FDA and /or EU Directive regulations, ICH Guidelines and local regulatory requirements
• Basic knowledge of three to five therapeutic areas, sufficient to function as a CRA or have an in-depth knowledge of two to three therapeutic areas
• Thorough understanding of standard operating procedures
• Proficiency in Microsoft Office, eCRF, and IVRS packages

Employment type: Full Time, Home based, Permanent