They have a range of studies running at the clinic suitable for those with varying degrees of Memory Impairment, Alzheimer’s disease and Dementia.
They are looking for an ambitious individual for a Research Administrator role. If you are looking to begin a career with an interesting and growing company, please get in touch.
Duties will include
Key Responsibilities:
General Administration Tasks
Assist the team with creation of study packs, documents, and maintenance of site files and consent logs
Assist with the provision of documents to Sponsors/CRA’s
Ensure all required certificates for the team are kept up to date
Assistance with tracking trials and appointments through Excel.
Retrieving and organizing patient notes and files using CTMS (Clinical trial monitoring systems)
Assistance with preparation for audits and reviews.
Photocopy, filing and general support.
Carry out day to day duties and responsibilities using various digital platforms such as Microsoft Teams, Excel, Word, Outlook and PowerPoint.
Electronic Data Capture
Liaise with Study Coordination Director regarding adverse events and if necessary, enter the recorded event onto the electronic data system (EDC) and fax forms to sponsor company.
Monitor the EDC system on a daily basis for any queries and liaise with team members as appropriate.
Liaise with medical staff regarding queries, errors, missing information ensuring a response has been provided.
Carry out online training for each new study in order to understand, navigate and access study portals.
Liaise with sponsor company monitors during site visits to ensure any generated queries/missing information has been added to EDC in a timeous manner.
Well organized person. Be willing to embrace new tasks. Have a good work ethic. Strong and encouraging communication skills. Great telephone manner. Attention to detail and accuracy. Work well and establish good rapport within the team. A can do attitude.