*Clinical Research Physician *Please learn the next job description totally to make sure you’re the fitting match for this position earlier than making use of.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 introduced in a possible chronological order i.e. the main target of labor progresses down the specification with seniority.* Requirements: ** *Medical Doctor UK Trained** *FY1 & 2 accomplished ** *2 years publish 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 examine.* To carry out medical screening on wholesome volunteers and sufferers together with medical historical past taking, bodily examination and assessment of laboratory reviews in accordance with the examine protocols.* To collate essential medical paperwork and knowledge to make knowledgeable choices about inclusion onto a medical trial.* To assessment all Case Report Forms with regard to inclusion/exclusion of topics previous to graduation of the examine.*Clinical trials procedures** To be conversant in all present examine protocols.* To talk about protocols in-house and with sponsors and consultants.* To supervise all security points throughout the research.* To preserve data, understanding and follow of normal medical follow and to take care of Advanced Life Support abilities.* 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 assessment and analyse security, pharmacokinetic and pharmacodynamic information and current the findings in interim reviews.* To take part within the discussions concerning the affect information 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 applicable throughout the conduct of ongoing research.* To write Patient Information Leaflets/Informed Consent Forms for deliberate medical research.* To assessment examine protocols and to take part within the technology of examine protocols as required.*Regulatory work** To write related sections of Patient Information Leaflets/Informed Consent Forms. * To assessment and contribute to the event of Investigator’s Brochures when required.* To assessment and implement advice from scientific advisory conferences into related examine paperwork in preparation for submission.* To take part in discussions with scientific and different consultants in preparation for regulatory submissions.