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Research Physician Human Medical Trials

Census Recruitment Ltd
Job LocationLondon
EducationNot Mentioned
Salary£64,000 - £75,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

RESEARCH PHYSICIAN- Medical DoctorPharmaceutical Human Trials and TestingCentral London£63,000-£70,000 (year 1)Our client is one of the UKs leading Pharmaceutical Research and testing centres. Based in central London and connected to a major hospital. The business is mainly involved in Human Trials on healthy patients and we are currently looking for Medical Doctors with an interest in the field of medicinal research and testing.Ideal candidates will have at least 2 years post foundation practice. We are open to all applicants who are qualified and experienced MDs looking for a new direction.Exceptional communication is a key, and you will be provided with first class conditions and generous financial package.We openly welcome Ex-Military doctors to apply.Responsibilities:The job specification below shows the breadth of work covered by the Research Physicians and Senior Research Physicians. The focus of an RP’s work is expected change with seniority. In general, the specification shown below is presented in a probable chronological order i.e. the focus of work progresses down the specification with seniority.1. Volunteer screening in preparation for clinical trials

  • To obtain informed consent from subjects prior to inclusion into a study.
  • To perform medical screening on healthy volunteers and patients including medical history taking, physical examination and review of laboratory reports according to the study protocols.
  • To collate necessary medical documents and information to make informed decisions about inclusion onto a clinical trial.
  • To review all Case Report Forms with regard to inclusion/exclusion of subjects prior to commencement of the study.
  • To liaise closely with volunteers and patients enrolling for clinical trials, their relatives if necessary.
  • To liaise with volunteers’ and patients’ own doctors, including specialist staff, when required.
  • To liaise closely with the recruitment staff regarding screening status, drop outs, withdrawals, replacements, follow-up appointments etc.
  • To maintain detailed reports of all screened volunteers and communicate screening progress to relevant departments.
    • 2. Clinical trials procedures
  • To be familiar with all current study protocols.
  • To discuss protocols in-house and with sponsors and experts.
  • To supervise all safety aspects during the studies.
  • To maintain knowledge, understanding and practice of general medical practice and to maintain Advanced Life Support skills.
  • Evaluate and treat all Adverse Events that arise during studies and prepare safety reports.
  • To ensure a safe discharge from the unit and to conduct follow-up examinations after completion of the study.
  • To participate in and supervise (as member of Project Teams) study procedures as drug administration, safety measures and other study methodology.
  • To keep up to date with all Research Unit activities through regular participation in study-related meetings in the unit.
  • To keep up to date with relevant ICH GCP issues and developments and to adhere to them at all times
  • To work to RPL Standard Operating Procedures (SOPs), laws, guidelines and rules at all times.
  • To co-operate with the Training Department and the Quality Assurance and Monitoring Departments in the maintenance of records for the preparation of audits, inspections and other visits.
  • Ensure accurate and complete recording of data
  • To collaborate with the Quality Control (QC) and Data Management (DM) departments and external monitors to resolve data queries.
    • 3. Reporting
  • To produce and update case reports for volunteers who experience Serious Adverse Events or other notable Adverse Events.
  • To review and analyse safety, pharmacokinetic and pharmacodynamic data and present the findings in interim reports.
  • To participate in the discussions regarding the impact data in interim/safety reports has on clinical trial progression.
  • To assist with the review and analysis of data at the end of clinical trials and subsequently be involved in the writing of final medical study reports.
  • To assist with the writing of any other medical or study reports that may be required, e.g. with relation to investigations, results obtained or study methodology.
    • 4. Medical writing
  • To contribute to the writing of Study Operations Manuals for upcoming studies and update as appropriate during the conduct of ongoing studies.
  • To write Patient Information Leaflets/Informed Consent Forms for planned clinical studies.
  • To review study protocols and to participate in the generation of study protocols as required.
  • To actively contribute to the review and updating of RPL’s SOPs and produce UPIRs when required.
  • To assist in the production of proposals for future studies, which may include presentations to clients.
    • Required skills
  • Clinical Trials
  • Examination
  • Foundation
  • Quality Control
  • Physicians

    • Keyskills :
    Clinical Trials Examination Foundation Quality Control Physicians

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