Hobson Prior

Jobs from Hobson Prior

London (On site) · Full time

Hobson Prior is seeking an Administrative Assistant to provide comprehensive support to senior leaders within the Global Medical & Scientific Affairs Oncology Therapeutic Area. This role requires a proactive individual who can manage priorities independently and resolve issues efficiently. The successful candidate will work closely with various internal and external stakeholders and integrate seamlessly with [...]Read More... from Administrative Assistant – III See details

Uxbridge (Remote) · Full time

Hobson Prior is seeking a highly motivated Medical Affairs Manager to join the Global Medical Affairs team at a well-known pharmaceutical company. This role focuses on person-centric HIV care and treatment. You will support current HIV Daily Oral Treatment strategies and work collaboratively with various teams. This is a 9-month contractor role based in Uxbridge, [...]Read More... from Medical Affairs Manager See details

London (On site) · Full time

Hobson Prior has partnered with a biotechnology company who is seeking a Validation Specialist to join our clients team in London. In this role, you will support the Engineering department to ensure our gene therapy manufacturing activities comply with validation standards. Please note that to be considered for this role you must have the right [...]Read More... from Validation Specialist See details

Oxford (On site) · Full time

Hobson Prior is seeking a Stat. SAS Programmer to join a well know biotech company. This role involves providing stat. programming support for the creation and enhancement of medical products, including research and clinical studies. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: [...]Read More... from Statistical SAS Programmer See details

London (On site) · Full time

Hobson Prior is seeking a dedicated and experienced Senior Quality Specialist to join a pharmaceutical company in London. In this role, you will play a crucial role to maintain the company’s Quality Management System and release activities for clinical trial supplies in compliance with Good Manufacturing Practices. Please note that to be considered for this [...]Read More... from Senior QA Specialist See details