Clinical Research Physician The job specification under exhibits the breadth of labor coated by the Research Physicians and Senior Research Physicians inside. The focus of a Research Physician work is predicted change with seniority. In normal, the specification proven under is offered in a possible chronological order i.e. the main focus of labor progresses down the specification with seniority. Requirements: Medical Doctor UK Trained FY1 & 2 accomplished 2 years submit basis expertise Motivated to get into business Volunteer screening in preparation for medical trials To get hold of knowledgeable consent from topics previous to inclusion right into a research. To carry out medical screening on wholesome volunteers and sufferers together with medical historical past taking, bodily examination and evaluation of laboratory reviews based on the research protocols. To collate vital medical paperwork and knowledge to make knowledgeable choices about inclusion onto a medical trial. To evaluation all Case Report Forms with regard to inclusion/exclusion of topics previous to graduation of the research. Clinical trials procedures To be accustomed to all present research protocols. To talk about protocols in-house and with sponsors and specialists. To supervise all security facets in the course of the research. To preserve information, understanding and follow of normal medical follow and to keep up Advanced Life Support expertise. Evaluate and deal with all Adverse Events that come up throughout research and put together security reviews. Reporting To produce and replace case reviews for volunteers who expertise Serious Adverse Events or different notable Adverse Events. To evaluation and analyse security, pharmacokinetic and pharmacodynamic knowledge and current the findings in interim reviews. To take part within the discussions relating to the influence knowledge in interim/security reviews has on medical trial development. Medical writing To contribute to the writing of Study Operations Manuals for upcoming research and replace as acceptable in the course of the conduct of ongoing research. To write Patient Information Leaflets/Informed Consent Forms for deliberate medical research. To evaluation research protocols and to take part within the technology of research protocols as required. Regulatory work To write related sections of Patient Information Leaflets/Informed Consent Forms. To evaluation and contribute to the event of Investigator’s Brochures when required. To evaluation and implement advice from scientific advisory conferences into related research paperwork in preparation for submission. To take part in discussions with scientific and different specialists in preparation for regulatory submissions.