FAQs
What is the main focus of the Research Administrator role?
The main focus of the Research Administrator role is to conduct audits of clinical trial data within the Research and Development Department.
What qualifications are required for this position?
While specific qualifications are not detailed in the job description, candidates should possess excellent organisational, prioritisation, administrative, and communication skills, along with a good eye for detail.
Is experience in clinical research necessary?
The job description states that the ideal candidate should be highly motivated and passionate about clinical research, but it does not specify if prior experience is mandatory.
What kind of tasks will the Research Administrator be responsible for?
The Research Administrator will work across various computer systems, ensure paperwork is correctly recorded, and facilitate communication between consultants, nurses, clinical teams, and trial sponsors.
Should applicants expect to work independently?
Yes, candidates are expected to be able to undertake tasks on their own initiative and build effective working relationships.
Who can I contact for more information about this role?
For more information, you can contact Sarah Knight at sarahknight2@nhs.net.
Are there opportunities for career growth in this role?
Yes, this position is part of a growing research portfolio at Torbay Hospital, suggesting potential for further career growth and involvement in varied clinical trials.
What is the working environment like for the Research Administrator?
The working environment is described as friendly and supportive, with a team of various research professionals.
Are there any specific IT skills required for this position?
Yes, a high degree of IT skills is essential for managing multiple computer systems related to clinical trials.
What methods of communication are important in this role?
Effective communication between various stakeholders, including clinical teams, trial administration, support departments, and patients, is crucial to ensure the accuracy and timely uploading of trial patient data.