Maintain consistent high standard of detailed documentation including data collection and entry using paper and electronic case report forms. Competent in working on a variety of computer-based systems. Ability to read, interpret & understand research protocols. Can obtain written informed consent for research studies or willing to learn.
Obtains and records observations such as vital signs, ECG, respiratory function and blood glucose analysis, as required by the trial protocol and as delegated by the registered healthcare practitioner, informing trained staff of any abnormal results. Demonstrate proficiency in basic laboratory skills including venepuncture and effective management of laboratory samples, including processing, storage and coordinating shipment of samples; training will be provided if required.
Coordinates the implementation and assumes responsibility for aspects of clinical trial protocols in accordance with relevant guidelines, under direct and indirect supervision. Work both autonomously and as part of the research team in clinical areas within the trust and with external organisations.
Supports research participants through the process of trial participation. Provides a high standard of clinical care within a multi-professional research team, seeking assistance from registered healthcare professionals as appropriate. Demonstrate excellent communication skills to communicate effectively with all disciplines of staff, attending MDT meetings, investigator meetings, and other research events on and off site. Recognise emergency situations and respond appropriately in line with Trust policies and Standard Operating Procedures.
Current GCP certification or willing to complete. Demonstrate ability to meet trust values.
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Obtains and records observations such as vital signs, ECG, respiratory function and blood glucose analysis, as required by the trial protocol and as delegated by the registered healthcare practitioner, informing trained staff of any abnormal results. Demonstrate proficiency in basic laboratory skills including venepuncture and effective management of laboratory samples, including processing, storage and coordinating shipment of samples; training will be provided if required.
Coordinates the implementation and assumes responsibility for aspects of clinical trial protocols in accordance with relevant guidelines, under direct and indirect supervision. Work both autonomously and as part of the research team in clinical areas within the trust and with external organisations.
Supports research participants through the process of trial participation. Provides a high standard of clinical care within a multi-professional research team, seeking assistance from registered healthcare professionals as appropriate. Demonstrate excellent communication skills to communicate effectively with all disciplines of staff, attending MDT meetings, investigator meetings, and other research events on and off site. Recognise emergency situations and respond appropriately in line with Trust policies and Standard Operating Procedures.
Current GCP certification or willing to complete. Demonstrate ability to meet trust values.
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