Clinical Research Fellow - London, United Kingdom - St George's Healthcare NHS Foundation Trust

Tom O´Connor

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Tom O´Connor

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Description

To be the main point of contact for patients and participants in this research To identify and recruit patients, ensuring that each patient fulfils the study criteria and effective informed consent is obtained.

To ensure that the study is conducted strictly in accordance with the study To identify barriers to recruitment and ensure the Chief Investigator/supervisors are made aware of these.

Identify and implement action plans as required.

To ensure that all data is recorded accurately and complies with the requirements of the study protocol and the Data Protection Act.

To work in conjunction with senior colleagues in preparing submissions to the Joint Research Office and Ethics Committees.

To lead the production of high-quality peer-reviewed publications and national/ international presentations as required by the funding body or for dissemination to the wider academic community.

To lead relevant meetings associated with the research project or related To liaise with the funding company to ensure that the correct signals are processed, and that all required information are accurately and completed collected.

To perform statistical analysis of the data collected and provide detailed Clinical & Professional To maintain clinical expertise relevant to the ongoing To monitor patients condition throughout their participation and ensure any ensuing clinical needs are promptly treated or appropriately referred.

To observe the confidentiality of patient data at all times in accordance with the Data Protection Act. To provide ongoing information, education and support to participants regarding this clinical study.

To work as part of the research and multidisciplinary team and contribute to the ongoing development of the Research Institute.

To adhere to clinical protocols for the Research Institute, SGUL and NHS Trust and partner organizations (where applicable).


To adhere to SGUL CRF SOPs, policies, guidelines and current legislation including Health and Safety, Equal Opportunities, Data Protection, Intellectual Property and No To be responsible for management of own time and Administration To ensure that clinical study records are accurately To access computer network as required retrieving and inputting relevant To participate in relevant professional activities, such as departmental research Personal, Education, Training & Development To keep up to date with NHS, SGUL and EU developments for the implementation of clinical research To take part in the NHS Training & Education Programme as appropriate To keep up to date with current and potential research and information relevant to the care of patients in the clinical areas.

To maintain current knowledge by attending relevant courses and conferences, in particular the CPF and GSSP lectures held by the University.

To undertake 6 monthly progress review, and regular meetings with To identify learning needs in relation to specialist area of Ensure that all relevant health care professionals are educated and supported as required, enabling them to care for women in clinical studies.

To contribute to the Clinical Research Group meetings and discussions regarding research, training and education.

To continue your own professional development, keeping updated with current practice and maintaining a research degree portfolio.

Staff Management and Development To act as a resource and role model to less experienced staff and other members of the research team.

To facilitate and maintain effective communication within the research Other Duties To undertake such duties as may be required from time to time as are consistent with the responsibilities of the grade.

To work on related research projects, as deemed appropriate to Grade and Clinical Skills To cross cover appropriately for colleagues in their absence

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