Location
Guy's Hospital, Great Maze Pond, London

Hours
Full Time (hours not specified)

Salary
£38,488 per annum

About the Role
As a Clinical Research Practitioner, you will provide excellent customer care ensuring patients and participants are prioritized. You will work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice) to ensure strict adherence to clinical trial protocols. You will lead on a portfolio of clinical trials, coordinating participation by liaising with clinical teams to organise trial-specific investigations according to protocol requirements. Key responsibilities include accurate data collection, dissemination, and version control of essential documentation. You will devise, implement, and evaluate recruitment strategies for clinical studies, identifying eligible participants and gaining permissions for research contacts. For specific studies, you may be delegated to obtain consent from participants in line with Trust policy and research protocols. You will organise and facilitate participant appointments and follow-up communications, update participant study and medical records to document study-related activities, and ensure confidentiality of all information. Additionally, you will complete case report forms accurately and timely, transcribing relevant clinical data from medical notes and study files, and maintain the Investigator Site Files.

Experience
Experience working within clinical research settings and familiarity with clinical trial protocols and regulatory requirements is essential. Proven ability to coordinate multiple trials and liaise effectively with clinical teams is required.

About you
You should have excellent customer care skills, be highly organized, detail-oriented, and able to work independently while maintaining strong communication with multidisciplinary teams. A commitment to maintaining confidentiality and working within ethical guidelines is essential.

Qualifications
Relevant qualifications or experience in clinical research or healthcare are expected. Knowledge of ICH GCP guidelines and clinical trial governance is required. Specific training or certification related to clinical research may be advantageous.