Taking forward a portfolio of clinical trials from a recruitment perspective which will include the set up of recruitment documentation, providing updates to the Recruitment Manager, Study team and Sponsor, and completing close down / recruitment update reports. Develop and build on the Consent 4 Consent (C4C) initiative. Inputting data into the C4C database. Compiling reports for Research Governance purposes. Receiving and placing calls from and to potential study participants. Enter medical history and demographic information from potential study participants into computerised systems. Communicate study information to potential participants, as required. Telephone screen participants according to the scripts provided for each study. Make recommendations for process improvement. Assist in training new employees and new researchers with the C4C process. Assist and develop recruitment information on the CRF website and social media accounts. Assist with obtaining medical reports from General Practitioners. Support other departments, as required. Assist in development and maintenance of recruitment strategies and trackers as required. Attend internal and external events to recruit participants / raise awareness of research as required. Participate and assist in developing continuing education plan directed at improving skills and facilitating personal and unit growth. Performs other related duties as assigned.