Clinical Engineering DepartmentLocation: Great Falls, MTJob Type: Temp/ContractReference Code: StafferLink-4491857Start Date: 11/20/2020Hours: Part TimeJob Category: Clinical Engineering Department

Assist in the management of patients and provide back-up support to the consultant.Initial and ongoing assessment of patient's medical, physical, and psycho-social status.Provide patient education and counseling covering health status, test results, disease processes, and discharge planning.Work with other members of the health care team to provide direct medical care to patients.Aware regarding patient Investigation profile/reports/plan, Treatment details/drug procurement, Drug allergies/patient history.To ensure timely attention and intervention for any query or requirement from the IP patient.Complete all OP & IP records on time with accuracy.

Assist in the management of patients and provide back-up support to the consultant.Initial and ongoing assessment of patient's medical, physical, and psycho-social status.Provide patient education and counseling covering health status, test results, disease processes, and discharge planning.Work with other members of the health care team to provide direct medical care to patients.Aware regarding patient Investigation profile/reports/plan, Treatment details/drug procurement, Drug allergies/patient history.To ensure timely attention and intervention for any query or requirement from the IP patient.Complete all OP & IP records on time with accuracy.

Assist in the management of patients and provide back-up support to the consultant.Initial and ongoing assessment of patient's medical, physical, and psycho-social status.Provide patient education and counseling covering health status, test results, disease processes, and discharge planning.Work with other members of the health care team to provide direct medical care to patients.Aware regarding patient Investigation profile/reports/plan, Treatment details/drug procurement, Drug allergies/patient history.To ensure timely attention and intervention for any query or requirement from the IP patient.Complete all OP & IP records on time with accuracy.

Assist in the management of patients and provide back-up support to the consultant.Initial and ongoing assessment of patient's medical, physical, and psycho-social status.Provide patient education and counseling covering health status, test results, disease processes, and discharge planning.Work with other members of the health care team to provide direct medical care to patients.Aware regarding patient Investigation profile/reports/plan, Treatment details/drug procurement, Drug allergies/patient history.To ensure timely attention and intervention for any query or requirement from the IP patient.Complete all OP & IP records on time with accuracy.

Research Systems Manager (Band 6)Main Area: Clinical ResearchSite: Musgrove Park HospitalTown: TauntonHours: Full time - 37.5 hours per weekGrade: Band 6The Trust research portfolio is thriving with new areas being developed each year. The Trust is sponsoring more studies and extending the scope of its local, national and international collaborative projects.The Department of Clinical Research has an exciting opportunity for someone with advanced level IT and systems development experience together with great organisational and people skills to be responsible for the development, maintenance and administration of research databases (primarily Edge) together with other information and data management systems.The post holder will be a key member of the Trust’s Research and Development team, ensuring the timely implementation of R&D Information Systems, effective monitoring and reporting of all data regarding research activity, with an emphasis on quality assurance.To succeed in the role you will need to be self-motivated and independent, preferably with considerable familiarity with Edge, primarily as a systems developer but with an understanding of the perspective of users and an ability to provide targeted training and support. Knowledge of research governance processes and procedures, with demonstrable knowledge of Good Clinical Practice (GCP) and the Health Research Authority (HRA) approvals process will be advantageous but a comprehensive training package will be provided.Our values are simple: Outstanding Care, Working Together, Listening and Leading.

Collect and coordinate information and compile regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy.Preparation & compilation of dossier in ACTD, CTD & country specific format according to guidelines of various countries.Response to query/deficiency/Notice of Deficiency raised by Drug Regulatory Authority or technical representative.Coordination with Quality Control, Quality Assurance and Production department for regulatory documents.Timely compile documents for license renewals, update and re-registrations.Maintain regulatory files/database and chronologies in good order.

planning and organising production schedulesassessing project and resource requirementsestimating, negotiating and agreeing budgets and timescales with clients and managersensuring that health and safety regulations are metdetermining quality control standardsoverseeing production processesre-negotiating timescales or schedules as necessaryselecting, ordering and purchasing materialsorganising the repair and routine maintenance of production equipmentliaising with buyers and marketing and sales staffCandidate must have experience in sales of agrochemical , pesticides, herbicides, crop care and related product line.

Should be fully conversant.Good Manufacturing guidelineGood Engineering Practice guidelineGood Leadership & Communication skill both Verbal & writtenEnglish is MUSTCandidate must have experience in sales of agrochemical , pesticides, herbicides, crop care and related product line.

You will ensure achievement of budget, New product launches & Retention / Development of team of ABM's & MR's. and achieving high PCPM and target achievement. You will handle scientific / medical promotions and effective implementation of strategies. You should be good in Man/ Management and Administrative Control on Field Force.