Senior Clinical Research Associate (SCRA) - Homebased, UK

This permanent SCRA is responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with 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

Successful candidates will have the following:

• Minimum of 2 years of previous independent field monitoring experience (required)
• Four-year life science degree preferred (or advanced degree)
• Thorough understanding of clinical research principles and process
• Thorough understanding of EU Directives and regulations, ICH Guidelines and local regulatory requirements
• Proficiency with IxRS, EDC systems
• Basic knowledge of three to five therapeutic areas, sufficient to function as a CRA and Strong Phase I and Oncology experience required
• Willingness to travel (required)
• Valid current passport required
• Driving license required
• Fluent in the local languages of the countries under responsibility and proficient in both spoken and written English