Anthonia Jones

Experience

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  Mecure Laboratory

  Sept 2010 - Aug 2011

  Trainee CTA/CRA (university Placement)

  Assisting research Nurses and Physicians in the planning and conduction of clinical trials.• Liaising with study volunteers and investigators to facilitate the efficient running of the study,• Performing clinical tasks and maintaining records when a trial is in progress.• Monitor the conduct of clinical trials, especially enrolment and quality of data.• Verify subject safety and site adherence to Regulations and ICH-GCP Guidelines.• Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up activities are conducted as necessary.• Review Informed Consent Documents and query language/narratives.• Acquire specific clinical and therapeutic knowledge related to studies monitored.• Conduct Qualification, Initiation, Interim and Closeout monitoring visits.• Working as part of a team running the department with colleagues.• Arranging & participating in the organisation of Investigator Meetings & Study Team Meetings. Taking minutes & distributing.• Assist with the Ethics / Regulatory Submissions; keeping a track of submissions & approvals for the study.• Preparing Protocols, Investigator Brochures and CRFs, which includes keeping track and re-ordering supplies.• Preparing the list of on-going trials using available template.• Managing and maintaining study documents & trial supplies e.g.; Patient Information Sheets, Patient Diaries, Lab Kits & Medical equipment for sites.• Preparing essential clinical trial documentation, distributing, tracking and filing of documents on return. Show less

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  Gaotech

  Aug 2013 - May 2014

  Project Administrator

  • Booked and co-ordinated internal and external client meeting, took and documented minutes and maintained seamless communication channel between all parties involved.• Raising POs (purchase orders)• Liaising closely with team members to get up-to-date deployment information to ensure all records are accurate.• Worked on project analysis, budgets, and financial management across the project.• Managing third party supplier relations• Identify and qualifying designated contractor and suppliers.• Effective management of the stakeholder and sponsor groups through the Operations and Strategic Boards.• Supporting in the creation of Project Initiation Documentations, Project Mandates, Project Briefs• Identifying and establishing client objectives, working from a Project plans.• Planning the whole client fulfilment program with team managers and technical teams. Show less

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  Olympus KeyMed

  Jan 2015 - Mar 2016

  Team Leader- Medical Devices

  Managing my own direct report Ensuring my team members are adhering to health and safety regulations Carrying out health and safety audits Ensuring that my team are carrying out repairs within the required quality standard Conducting internal checks on medical devices to ensure they meet repair standards Conducting one to one meetings and setting individual objectives that are SMART Ensuring the departmental targets are met by setting goals Making calls to both internal and external customers to give feedback on repair status Accomplishments I have increased the team's awareness of health and safety I have ensured that my teams needs are met by communicating with other parties as required I also improved the departments KPI targets by developing new and effective work methods Skills Used Leadership Administrative Attention to detail Communication Organisation Setting priorities Listening Show less

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  Novella Clinical

  Mar 2016 - Dec 2018

  EU Study Start-Up and Document Management Associate
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  IQVIA

  Jan 2019 - now

  • Global Regulatory and start up manager

    Oct 2020 - now

  • Regulatory and start up manager

    Jan 2019 - Oct 2020