We are looking for an experienced Clinical Trial Manager to join our supportive team at the UKCRC registered (ICTU), where you will be responsible for all aspects of trial management and for the oversight of a Trial Monitor.
You will assist in the coordination of study set-up, putting robust monitoring plans in place, liaising closely with the Chief Investigators and PIs at other centres. You will oversee the progress and performance of investigator sites, including efficient recruitment and reliable data collection by implementing and adapting established ICTU systems to ensure the study is conducted in accordance with contractual agreements, trial protocol, trial-specific processes and systems, SOPs, regulatory and ethical requirements and ICH-GCP guidelines, as well as delivered to time and within budget constraints.
You will have:
1. A Bachelor’s degree or equivalent in a biomedical/ scientific field.
2. Proven clinical trial experience gained in multi-centre randomised trials, including in neonatal medicine
3. Proven experience of working on clinical trials utilising routine healthcare data, or equivalent
4. A willingness to travel within the UK as well as working flexibly outside of office hours on occasion
5. A supportive, inclusive team environment where your contributions matter.
6. An ideal opportunity to develop your skills and knowledge further at a world-leading institution and be part of our mission to use science for humanity.
7. Benefit from a sector-leading salary and remuneration package (including 39 days’ annual leave and generous pension schemes).
8. Access to a range of workplace benefits including a flexible working policy from day one, generous family leave packages, on-site leisure facilities and cycle-to-work scheme.
9. Interest-free season ticket loan schemes for travel.
Be part of a diverse, inclusive and collaborative work culture with various and resources to support your personal and professional