Clinical Research Fellow

The post-holder will

Support timely delivery of the clinical trial to required medical standards and in line with current guidelines and regulations; Support research participants, provide medical assessments and liaise with principal investigators; Consent research participants, collect their medical histories and other relevant clinical data; Be responsible for specific study-related medical decisions as agreed with the Study Principal Investigator; Perform clinical procedures as appropriate to the assigned study; Review study documentation and complete appropriate sections of Case Report Forms; Maintain accurate and accessible research records and medical notes; Provide medical input into integrated clinical, safety and statistical reports as requested; Provide medical input and review of study protocols and other related study documentation and participate in research meetings, study review meetings, and meetings with principal investigators and study sponsors; Maintain awareness and keep abreast of latest technologies in the medical field and share that knowledge with the CRF team; Prepare reports for submission to regulatory bodies, funders and medical and scientific journals as appropriate; Ensure personal Trust mandatory training is up to date; Develop and maintain computer skills to utilise available systems for the efficient management and administration of the day-to-day activities of the CRF; Any other duties as may be deemed reasonable by the senior team; To participate in clinical and other service activities with the object of ensuring a high standard of patient care.