Tasneem Rizvi

Experience

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  Eli Lilly and Company

  Aug 1996 - Aug 2000

  Clinical Research, Medical Information and Pharmacovigilance Co-ordinator

  Start up, closeout, monitoring, audit and documentation of clinical trialsProvision and management of Regulatory and Medical Information ServiceManagement of training and Pharmacovigilance ProgramPrinting and editing of newsletter and annual regional reportsProduct complaint handling and establishment and running of medical library

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  Aga Khan University

  Jan 2000 - Jan 2001

  Staff Pharmacist

  Management of Drug and Poison Information Centre, Hospital Formulary, Pharmacy and Therapeutic Committee, Clinical Rounds, Clinical Research, Institutional Review Boards, Departmental Publications.

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  ATCO Laboratories Limited

  Jan 2001 - Aug 2009

  I worked on this International Assignment and it was a very good experience to work in Exports section. Gained a lot and accomplished a lot. Business Unit Head-Pediatrics, Gynae, Diabetes, Exports; Development and implementation of business and marketing plansTraining and development of field force including efforts for team buildingDevelopment and reinforcement of business plansDevelopment and execution of launch plans for new productsManagement of training and Pharmacovigilance Program

  • Business Unit Head-Based at Colombo Sri Lanka

    Jun 2008 - Aug 2009

  • Business Unit Manager

    Jan 2001 - Jan 2009
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  ZAFA Pharmaceuticals

  Sept 2009 - Aug 2010

  Chief Operating Officer-Soft Gelatin and Paediatric Division

  Managing operations of Soft Gelatin and Pediatric Division

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  University of Tasmania

  Oct 2015 - Nov 2021

  Presentation of research study Antimicrobial Stewardship in Community Settings

  • PhD Doctor of Philosophy (The Role of Community Pharmacist in Antimicrobial Stewardship)

    Oct 2018 - Nov 2021

  • Higher Degree by Research Masters-Clinical Pharmacy

    Oct 2015 - Nov 2018
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  Department of Health, Tasmania

  Aug 2021 - now

  Clinical Research Officer

  -Preparation and submission of new clinical research projects documents and amendments to ongoing clinical trial documents to the Research Governance Office and Human Research Ethics Committees. -Liaison with contract research organisations and pharmaceutical companies on all start upprocedures for new trials, including assisting with the negotiation of contract budgets with sponsors andhospital departments involved in the trial and preparation of all study start up documents.-Liaison with investigators, nurses, patients, community health services, business managers, departments, governing bodies, contract research organisations and pharmaceutical sponsor companies onall administrative processes associated with the trials.-Maintenance of all files and documents with strict confidentiality and accuracy, as required by the National Health and Medical Research Council, contract research organisations and the Good Clinical Practice Guidelines.- Maintain a high standard of accuracy and integrity of several online databases used for collecting patient information, including entering all data required and responding to queries generated by contract research organisations.- Assist with patient clinical trial visits as required.- Attend Investigator meetings and training sessions associated with protocol, database management, safety and Good Clinical Practice training as and when required.-Support with research activities within the clinical trial's unit, including tasks associated with theallocated clinical trials protocols.-Undertakes all functions associated with the creation and maintenance of comprehensive databases and registries and work towards achieving the objectives of the unit. Show less

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  Department of Health, Australia

  May 2023 - now

  Teletrial Coordinator

  Supporting harmonisation activities to increase the uptake of the Australian Teletrial Model in Tasmania.Ensuring effectiveness and efficiency of local policy and procedures to support Tasmanian Regional Clinical trial Coordination Centre to align seamlessly with the evolving landscape of clinical research. A significant aspect of my responsibilities is to design and implement supervision plans for Teletrials. To engage and liaise with investigators, study coordinators, HREC Administrators, and RGOs, enabling them to conduct their research endeavours efficiently while upholding the highest ethical standards mandated by the National Clinical Trials Governance Framework regarding teletrials. Support stakeholders and networks engaged in research and sponsored clinical trials across Tasmania in advancing the realm of clinical research, contributing significantly to scientific knowledge and healthcare improvements through teletrials. Show less

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  University of Tasmania

  Apr 2024 - Sept 2024

  Clinical Trial Research Officer • Wicking Dementia Res Educ Ctr

  Wicking Dementia Research and Education