Development Scientist - Assay Development (Clinical Trials)

About the Role

hVIVO are seeking a Development Scientist to join our team of scientists who are responsible for the development and validation of molecular, virology, microbiology, and immunology assays in line with hVIVO corporate objectives and priorities.

This role is on site full time at our facility in Canary Wharf, E14.

The Development Scientist will also lead bespoke R&D client projects as part of lab services and contribute to the business and lab capabilities development strategy, engaging directly with clients as required.

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.

Key Responsibilities

• Provide scientific expertise and delivery in the development and validation of assays to enhance hVIVO business potential;
• Be responsible for the delivery of internal and client contracted research projects;
• Prepare and review study protocols, data, and final reports for both Clinical and hLab studies;
• Report analysed data within the department, to clients, and to other divisions, as required;
• Manage time effectively to meet competing demands, ensuring that work is prioritised and that outputs are delivered to defined deadlines;
• Establish budgets and determine resource needs for experimental work;
• Provide regular updates on progress to management, compiling large data sets into presentable formats;
• Provide training and mentoring for junior staff and new technologies and processes within the lab;
• Management of the operational delivery of multiple projects across the team;
• Liaise with the QA department to ensure timely auditing of study documents, study results, and routine system procedures;
• 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 writing and reviewing publications to showcase hVIVO research in appropriate peer-reviewed journals;
• Management and review hVIVO SOPs regularly to ensure scientific robustness and/or change in regulatory guidelines;
• Assist in the maintenance of the laboratories and ensure all procedures are performed according to Health & Safety regulations;
• Attend conferences, client meetings, and lectures as appropriate