The successful candidate will be responsible for maintaining organisational systems within the team, assisting in training coordination, and providing updates on recruitment status for studies. Collaboration with research teams and ensuring the timely collation and reporting of trial data are key components of the role. The position requires adherence to research governance and ethics guidelines, with ongoing training provided to meet the needs of the role.
An exciting opportunity has opened up to join the Clinical Research Team with the main purpose of the role to assist the with all aspects of administration related to clinical trials according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies.
You will provide support to the Clinical Research Nurses in daily research activity, patient communication and assist in workload management.
You will join an enthusiastic well established Gastroenterology team, comprising of 3 Research Nurses, 1 Research Practitioner and 2 Research Assistants. We conduct a range of Commercial and Non-Commercial Academic studies for patients with Inflammatory Bowel Disease.
- Typing and formatting of letters and reports where appropriate; meeting timescales as directed by your line manager.
- To take minutes of meetings, type and distribute to all members of staff and to follow up actions as required.
- Word processing, which may include letter, memos, notes, record cards, messages and email communication.
- Collate, provide, receive and appropriately store (manually and electronically) sensitive and confidential information.
- Maintain administrative systems set up in team offices to ensure an organised and efficient working environment for staff.
- Responsible for assisting with the booking of team training and responsible for maintaining local training records
- Undertake reception duties
- Provide research teams, research networks/themes, and R&I
- Management team with up to date information about recruitment status of study. Ensure information is available and accessible.
- Ensure that the accrual figures for studies and referred patients are collated and sent to the trial co-ordinating centre, and R&IManagement team for all studies according to agreed timescales.
You will be expected to work at all times according to regulations described in ICH Good Clinical Practice and to the most current guidance relating to Research Governance and Research Ethics. Training needs will be identified and planned accordingly.
About us
To read more information about the advertised role, and the main job duties/responsibilities please open the Job Description and Person Specification located under the supporting documents heading. You can also read more information about working at the Northern Care Alliance within the attached Candidate Information Pack or by visiting our careers website: www.jobsincare.com/job/jbnsIzQo
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