May 19, 2021
We are looking for a Life Sciences graduate to join our dedicated Clinical Affairs Team. This is an excellent opportunity if you are someone who has experience in handling large quantities of data. You will be tasked with effectively supporting the data management requirements of clinical investigations at Perspectum.
You will be central to the oversight and management of data in relation to clinical investigations, having close interactions with all key functions. You will also work very closely with the Clinical Project Management team, supporting a number of active research projects. Perspectum has a dynamic research programme, Sponsoring an exciting portfolio of studies.
As a Data Operations Associate, you will take lead responsibility for reviewing and quality checking research data to ensure that all captured data follows the rules outlined by the ethically approved research protocol and associated data management plan. You will also prepare data entry guidelines, data management reports and other documents required for preparing and completing databases - these play an integral part in a clinical investigation’s data compliance. You will gain a thorough understanding of the full spectrum of elements involved in setting up a new research project, from conception to implementation to study management. You will also gain knowledge and confidence in the use of various software programs. These include the company’s Quality Management System, Clinical Trial Management System (CTMS) and the electronic data capture (EDC) platform that generates case report forms (CRFs).
If you are interested in research, then data management is a fantastic way of learning about the industry in-depth, as well as gaining a fluency in the running and compliance of clinical investigations.
To be successful in this role you will hold a degree in Life Sciences or another relevant field and have the ability to work well independently as well as part of a multidisciplinary team. You will be an excellent communicator written and verbally as well as an effective multi tasker in a fast paced environment. You will have excellent IT skills as well as high levels of attention to detail.
Although not essential, it would be desired if you have completed GCP training and have prior experience with clinical/medical data. Knowledge of FDA/ISO and GCP requirements as well as clinical investigations and data management practices would be a bonus.