The Development team are responsible for the development and validation of molecular, virology and immunology assays in line with hVIVO corporate objectives and priorities.
hVIVO is a dynamic and pioneering global player in the pharmaceutical early phase research sector, and has been recently developing a strong discovery (research and development) focus to investigate human disease to help find better treatments, faster. We are always interested to hear from similarly dynamic and pioneering individuals who share our vision to better understand the more precise nature of human disease and to really make a difference.
- Provide scientific expertise and support in the delivery of development and validation of virological and immunological assays;
- Responsible for the support in the delivery of internal and client contracted research projects;
- Manage time effectively to meet competing demands, ensuring that work is prioritised and that outputs are delivered to defined deadlines;
- Provide regular updates on progress to management;
- Ensure all work, where appropriate, maintains compliance with Good Clinical Practice and Good Clinical Practice for Laboratories, all relevant Standard Operating Procedures (SOPs) and company standards and guidance;
- Assist in the maintenance of the laboratories and ensure all procedures are performed according to Health & Safety regulations;
- Perform study administration tasks, for example lab book and label production, document scanning, filing or archiving.