Clinical Project Coordinator
Our growing and successful business comprises of over 900 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.
People join Quotient Sciences because we are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.
We have a fantastic opportunity for a driven and intelligent individual to join the Project Management team as a Clinical Project Coordinator. Within the Project Management team you will support in the completion of client projects to the agreed standards of quality, agreed timelines and within cost budgets.
The successful candidate should have excellent communication and customer service skills as in this role as the Clinical Project Coordinator you will be required to interact with clients and will also host on site client monitoring visits. In addition to this, you will be responsible for the preparation and management of study related documents. This will include the generation/review of study day paperwork and management of review, sign off and data query resolution of eCRF data.
Other responsibilities will include subject information leaflet writing, internal data generation for client reporting, managing data query resolutions and general support for the Project Management group.
In this position you are required to work effectively with colleagues across all functional areas, being able to build strong working relationships and to collaborate and influence with colleagues is key.
The ideal candidate will be educated to a minimum degree level qualification or equivalent and should have a high attention to detail and accuracy and will be focused on quality delivery. Some relevant work experience in a pharmaceutical company or CRO is essential for the role.
In return, you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.