£50 - £55 Per Hour
Research & Development
Pharmaceuticals / Biotechnology / FMCG

About The Role

My Client is a niche and growing CRO in the UK specialising in Respiratory medicine. They are currently in need of a Lead CRA to perform oversight activities for a single site study in the EU.

Main Responsibilities

Coordinate the steps which facilitate and streamline the activation and management of allocated clinical trials.
– Develop and/or maintain resources to support clinical trials, such as tracking logs, study manuals, Trial Master File (TMF)
– Data management including case report forms (CRF) design, data management plan(DMP), data entry, queries and cleaning, data reconciliation, quality control of database
– Support the conduct of allocated clinical trials through effective
communication with the team and our clients fostering collaboration with investigators
– Assist with the development and project management infrastructure and provide support for the Trial Project Management

Required Experience

– 5 – 7 Years’ experience in clinical research and data management

– Demonstrated understanding of Good Clinical Practice (GCP), regulatory, ethical, privacy and other relevant guidelines
– Understanding of medical terminology, ideally respiratory disease and virology

– Experience in Case Report Form (CRF)design

– Excellent organizational skills including the ability to establish and work within Clinical Research Associate timelines

– Demonstrated experience with Microsoft Word, Outlook, Excel, PowerPoint

– Demonstrated project management skills including the ability to work autonomously across multiple projects with tight timelines

– High attention to detail

– Ability to review processes and suggest improvements to enhance existing methods

– Excellent oral and written communication skills

– Personal confidence and demonstrated ability to liaise with professionals from a variety of backgrounds

– Able to work independently and as an effective member of a multi-disciplinary team

– Willingness to travel as required, when safe to do so