Clinical Academic definition

Clinical Academic means a medical practitioner employed by The University of Western Australia as a professor, associate professor, senior lecturer or lecturer and also employed by the Employer as a medical practitioner undertaking clinical service work.
Sample 1Sample 2Sample 3
Clinical Academic means a specialist registered by the Medical Board of Australia and who is employed in a Full Time capacity by a University in an academic role in the faculty of medicine (however described) and also employed by a Health Service.
Sample 1Sample 2Sample 3
Clinical Academic means a person who:
Sample 1Sample 2Sample 3

Examples of Clinical Academic in a sentence

  • This function will ultimately be taken on by Clinical Academic Groups within King’s Health Partners (rather than the Trust’s Divisions), as these become established across KHP.

  • Clinical Academic staffing levels in UK Medical and Dental Schools: data update 2004.

  • Adverse actions are classified as Clinical, Academic and Training Performance Adverse Actions or Disciplinary Adverse Actions.

  • Allied Health/Nursing Clinical Academic Appeals are for those appeals which deal specifically with clinical evaluation judgments.Copies of the policy and forms may be obtained through the Academic Division Offices, from the Dean of Academic Affairs, or by contacting the Academic Appeals Committee Chairperson.

  • Cardiol entered into a development agreement (the “Caro Development Agreement”) with the Clinical Academic Research Organization, S.A. DE C.V. (“Caro”) dated August 28, 2018, for the further research and development of proprietary drug formulations for the treatment of heart failure.

  • The Contract of Agreement will be signed by an appropriate NHS Lothian representative of Lothian’s Clinical Academic Pathways Partnership (who will normally be the award recipient’s mentor) on behalf of the Board.

  • Also Lecturer in Clinical Academic Research at University of Edinburgh which includes delivery of Masters Nursing in Clinical Research.

  • A Clinical Academic appointed as a Head of Department in a hospital shall have the same duties, obligations and allowance entitlements as are prescribed for Heads of Departments in the Medical Practitioners Industrial Agreement.

  • The services SLaM provides are organised into Clinical Academic Groups (CAGs) that offer the best care and treatment, based upon reliable research evidence.

  • Data analysis involved working with the10:20amExperiences of family members with critical care diaries in an intensive care unitPresenter: Miss Corrienne McCulloch, BSc (Hons), Senior Practitioner (Clinical Research), NHS Lothian/ University of Edinburgh, Edinburgh, UKBiographyCorrienne is currently undertaking a PhD part time at the University of Edinburgh as part of a Clinical Academic Research Career Scholar- ship with NHS Lothian and the University of Edinburgh.


More Definitions of Clinical Academic

Clinical Academic means a currently employed member of the academic staff of the University.
Sample 1Sample 2Sample 3
Clinical Academic. Means a specialist registered by the Medical Board of Australia and who is employed by a University as a Professor, Associate Professor, Senior Lecturer or Lecturer in the faculty of Health Sciences and also employed by the employing authority as a Clinical Academic performing duties which may include, but not limited to: • The provision of professional clinical services in the branches of medicine or areas of specialty which make up the employing authority’s clinical profile • Administrative functions associated with or inherent in the provision of clinical services • Supervision and management of the employing authority’s staff associated with the provision of clinical services, the employing authority’s research programs, teaching and training • Attendance at, and participation in, relevant standing or ad hoc committees associated with or inherent in the provision of clinical services • Design, implementation and maintenance of quality assurance and improvement procedures associated with or inherent in the provision of clinical services • Teaching and in-service training of the employing authority’s staff associated with or inherent in the provision of clinical services • Attendance at meetings related to teaching and training of staff • Support of relevant clinical research programs conducted by the employing authority • Participation, where relevant and required, in the employing authority’s on call and recall rosters related to the provision of relevant clinical services • Participation in the provision of outreach services and health education programs as required • Representing the employing authority in clinical and scientific meetings locally, nationally or internationally • Participation in programs designed to maintain or enhance personal professional competency.
Sample 1Sample 2
Clinical Academic is an employee who ordinarily holds a substantive contract with an HEI, and they are a qualified doctor or dentist (including those in specialist training) holding an active GMC or GDC registrations, and where relevant, a license to practice.
Sample 1Sample 2
Clinical Academic means staff of a university school of medicine who are also employed in the NSW Public Health System and provide clinical and associated administrative services for public patients in public hospitals. It excludes university staff who are medical practitioners but who do not become employees of the NSW Public Health System, as set out in policy directive PD2010_036 Clinical Academics Employed in the NSW Health Service
Sample 1Sample 2Sample 3
Clinical Academic. Means a specialist registered by the Medical Board of South Australia and who is employed by the University of Adelaide or Flinders University of South Australia as a Professor, Associate Professor, Senior Lecturer or Lecturer in the faculty of Health Sciences and also employed by the employing authority as a Clinical Academic performing duties which may include, but not limited to: • The provision of professional clinical services in the branches of medicine or areas of specialty which make up the employing authority’s clinical profile • Administrative functions associated with or inherent in the provision of clinical services • Supervision and management of the employing authority’s staff associated with the provision of clinical services, the employing authority’s research programs, teaching and training • Attendance at and participation in relevant standing or ad hoc committees associated with or inherent in the provision of clinical services • Design, implementation and maintenance of quality assurance and improvement procedures associated with or inherent in the provision of clinical services • Teaching and inservice training of the employing authority’s staff associated with or inherent in the provision of clinical services • Attendance at meetings related to teaching and training of staff • Support of relevant clinical research programs conducted by the employing authority • Participation, where relevant and required in the employing authority’s on call and recall rosters related to the provision of relevant clinical services • Participation in the provision of outreach services and health education programs as required • Representing the employing authority in clinical and scientific meetings locally, nationally or internationally • Participation in programs designed to maintain or enhance personal professional competency. CAEA 2009 of 29 5
Sample 1
Clinical Academic. Means a specialist registered by the Medical Board of South Australia and who is employed by the University of Adelaide or Flinders University of South Australia as a Professor, Associate Professor, Senior Lecturer or Lecturer in the faculty of Health Sciences and also employed by a health unit as a Clinical Academic performing duties which may include, but not limited to: • The provision of professional clinical services in the branches of medicine or areas of specialty which make up the health unit’s clinical profile • Administrative functions associated with or inherent in the provision of clinical services • Supervision and management of health unit staff associated with the provision of clinical services, health unit research programs, teaching and training • Attendance at and participation in relevant standing or ad hoc committees associated with or inherent in the provision of clinical services • Design, implementation and maintenance of quality assurance and improvement procedures associated with or inherent in the provision of clinical services • Teaching and inservice training of health unit staff associated with or inherent in the provision of clinical services • Attendance at meetings related to teaching and training of staff • Support of relevant clinical research programs conducted by health units • Participation, where relevant and required in the health unit’s on call and recall rosters related to the provision of relevant clinical services • Participation in the provision of outreach services and health education programs as required • Representing the health unit in clinical and scientific meetings locally, nationally or internationally • Participation in programs designed to maintain or enhance personal professional competency.
Sample 1

Related to Clinical Academic

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Clinical Trials means a controlled study in humans of the safety or efficacy of a Product, and includes, without limitation, such clinical trials as are designed to support expanded labeling or to satisfy the requirements of an Agency in connection with any Product Approval and any other human study used in research and Development of a Product.

  • Clinical Studies means human clinical trials for a Licensed Product and any other tests and studies for a Licensed Product in human subjects.

  • Clinical Trial means a Phase I Clinical Trial, Phase II Clinical Trial or Phase III Clinical Trial, or any post-approval human clinical trial, as applicable.

  • Clinical Study means a Phase I Study, Phase II Study, Phase III Study, or Pivotal Study, as applicable; but excluding any Post-Approval Studies.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Phase I Clinical Trial means a clinical trial conducted in healthy humans or patients, which clinical trial is designed to establish the safety, drug-drug interactions and/or pharmacokinetics of an investigational drug given its intended use, and to support continued testing of such drug in Phase II Clinical Trials.

  • Clinical peer means a physician or other health care professional who holds a non-restricted license in a state of the United States and in the same or similar specialty as typically manages the medical condition, procedure or treatment under review.

  • Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Phase 4 Clinical Trial means a Clinical Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • clinical evidence means clinical data and clinical evaluation results pertaining to a device of a sufficient amount and quality to allow a qualified assessment of whether the device is safe and achieves the intended clinical benefit(s), when used as intended by the manufacturer;

  • Phase 3 Clinical Trial means a pivotal clinical trial in humans performed to gain evidence with statistical significance of the efficacy of a product in a target population, and to obtain expanded evidence of safety for such product that is needed to evaluate the overall benefit-risk relationship of such product, to form the basis for approval of an NDA and to provide an adequate basis for physician labeling, as described in 21 C.F.R. § 312.21(c) or the corresponding regulation in jurisdictions other than the United States.

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Phase II Clinical Study means a human clinical study of a product initiated to determine the safety and efficacy in the target patient population, as described 21 C.F.R. 312.21(b).

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Phase II Clinical Trial means a controlled human clinical study that would satisfy the requirements of 21 CFR 312.21(b), conducted to study the effectiveness and establish the dose range of a Product for a particular Indication in patients with the disease or condition under study, including a Phase IIA Clinical Study or Phase IIB Clinical Study.

  • Nuclear fuel cycle-related research and development activities means those activities which are specifically related to any process or system development aspect of any of the following: - conversion of nuclear material, - enrichment of nuclear material, - nuclear fuel fabrication, - reactors, - critical facilities, - reprocessing of nuclear fuel, - processing (not including repackaging or conditioning not involving the separation of elements, for storage or disposal) of intermediate or high-level waste containing plutonium, high enriched uranium or uranium-233, but do not include activities related to theoretical or basic scientific research or to research and development on industrial radioisotope applications, medical, hydrological and agricultural applications, health and environmental effects and improved maintenance.

  • Biological diversity means the variability among living organisms from all sources including, inter alia, terrestrial, marine and other aquatic ecosystems and the ecological complexes of which they are part; this includes diversity within species, between species and of ecosystems.

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.

  • Phase III Clinical Study means a human clinical study of a product on a sufficient number of subjects that is designed to establish that such product is safe and efficacious for its intended use, and to determine warnings, precautions, and adverse reactions that are associated with such product in the dosage range to be prescribed, which trial is intended to support Regulatory Approval of such product, as described in 21 C.F.R. 312.21(c). 1.185. [***] 1.186. [***]

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Pivotal Clinical Trial means, with respect to a Licensed Product, (a) a phase 3 Clinical Trial or (b) any other clinical trial that is intended (as of the time the study is initiated) to obtain the results and data to support (without the need to conduct any additional clinical trial) the filing of an application for Regulatory Approval for such product.