Band 4 Clinical Trials Administrator inBirmingham inBirmingham PUBLISHED
FRI 13 DEC 2024
Key responsibilities include managing research databases, ensuring compliance with data protection and confidentiality policies, collating and transcribing data, checking patient recruitment and consent, and developing IT tracking systems for study documentation. The position requires excellent communication abilities, independent working skills, and strong planning and organisational capabilities to effectively manage a varied workload and collaborate with different stakeholders, including medical professionals, researchers, and external parties.
Are you an enthusiastic dynamic person wanting to work in Research as a Clinical Trials Administrator?
*In the Liver Research Delivery team, we have a position to join our team, if you are interested in working on a varied portfolio of liver diseases, this could be your opportunity to come and join us at Queen Elizabeth Hospital Birmingham.
*The Liver Research portfolio has an exciting range of commercial, academic, observational as well as complex interventional studies.
*You will have to opportunity to support the Research Nurses and Research Administration team to become part of an established delivery team with enthusiastic investigators.
*You will also have the opportunity to further develop administration skills, research systems knowledge, interpersonal communication, organisation, time management, & documentation skills.
For any information about the above post or you would like to come and meet us, please contact:
*Emma Burke or Diana Hull -- Senior Research Sisters on or or
*The post holder must be able to communicate information to a wide range of staff groups, i.e. Medical Consultants, Clinical Scientists, Researchers, Academics, Public and Patient groups and external stakeholders
*Liaise with Trust staff, managers and outside agencies involved in research in a professional and courteous manner
* To manage Research Databases, updating and developing them where necessary. The post holder will be expected to manage their own workload and to work independently, to collaborate with clinical and administrative staff to support the ongoing development of Database including advising of updates and errors as they arise
*To ensure compliance with Trusts and University policies on data protection, confidentiality and security
*To collate and transcribe /export data from medical and other records (paper or electronic) to CRFs (paper or electronic)
*To check recruitment of patients into studies including checking consent paperwork and study specimen records and to ensure that all relevant data has been recorded
*To develop IT tracking systems and ensure safe filing and storage of study documentation and samples in accordance with ICH GCP and research governance
The post holder must possess excellent communications skills and the ability to work on their own initiative as well as working in a team environment. This will require excellent planning and organisational skills using their own judgment to prioritise their workload effectively
About us
*Please Note : For a detailed job description for this vacancy, please see attached Job Description*
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