Experience

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  Mindwave Ventures

  • United Kingdom
  • IT Services and IT Consulting
  • 1 - 100 Employee

  • Product Manager, Products and Design Services

    • May 2022 - Mar 2024

    Mindwave is a health technology company that enables healthcare projects to take on user-centred design with an agile development approach, helping accelerate digital healthcare transformation with a personalised, human-focused view. Over the years, the team has grown from a handful of designers to a full-service provider, supplying PEPs/PHRs and other digital products alongside expert health design and technology consultancy.

  • Senior Project Manager

    • Nov 2020 - May 2022

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  Signant Health

  • Project Delivery Specialist

    • Jun 2019 - Oct 2020

    • Implementing electronic patient reporting outcome (ePRO) for clinical trial studies as per clients specified design on digital components such as web portal, App software, mobile and tablet devices.• Managing client expectations including capturing design requirements, working with developers to design ePRO platforms including data visualisation reports, ensuring all the internal and external quality checks are conducted and documented.• Ensuring the client expectations are met for via standard Key Performance Indicators (KPI) and Project Health reporting for renowned pharmaceutical, contract research organisations and biotechnology companies.• Responsible for overall client and project management and initiation of studies during all phases of a study, including timelines, budget, maintaining scope, risk management, quality (technical and user acceptance testing) and change requests using PMP methodology. Maintain clear visibility through project management and reporting tools for the overall status of the project and timelines.• Gathering user requirements across multi-function operational teams for key projects, transforming them into clear user stories for the development team. Conducting user acceptance testing by creating user scripts and assisting during client testing.• Responsible for creating, executing, and maintaining end user material through various formats such as printed materials, web-based material, or live presentations on location for varying audiences such as Pharmaceuticals, medical professional and patients.• Clinical data governance via data reconciliation for client’s clinical data platforms such as RAVE.• Supporting client to optimum ways of visualising data collection for strategic decision making.

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  Research Organisation (KC)

  • London, United Kingdom

  • Clincial Trial Management

    • Aug 2018 - May 2019
    • London, United Kingdom

    • Evaluating scientific proposals or protocols to identify logistical, regulatory and safety elements and implications.• Managing studies by establishing strong partnerships with external investigators and collaborators to ensure CO and ISR Agreements for financial.• Proactively identifying operational challenges and in collaboration with senior team members provides and implements solutions to ensure studies remain on track.• Maintains efficient collaboration with company’s Clinical Contracts and Finance (CCF) team and external investigator/study representative to ensure contracts are executed.Managing study drug planning and shipping activities with Materials & Logistics.• Implementing working processes to promote high quality, efficient, compliant systems for Late Phase research management and clinical Operations Quality Initiatives.• Maintaining internal Clinical Operations and Medical Affairs databases and clinical study data and document repositories.

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  Q² Solutions

  • London, United Kingdom

  • Project Coordinator

    • Mar 2017 - Jul 2018
    • London, United Kingdom

    • Affectively managing multiple stakeholder relationships including global counterparts through data management, monitoring and evaluating of studies – fidelity of the study to the protocol and to increase efficiency in the processes• Day to day management of studies through trouble shooting delays, liaising with different departments to ensure logistics and supply chain management• Communicating with study teams and clients to develop solutions for routine project related issues, participate in global improvement of the study with relevant process improvements• Facilitated and coordinated the work of multiple project teams engaged in the establishment and implementation of new projects to support the Project Manager
    • Update standard protocols rigorously, to match with organisational standards and client expectations

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  Chetanalaya

  • Delhi Area, India

  • Program Officer

    • Nov 2016 - Jan 2017
    • Delhi Area, India

    • Successfully delivered disability program within 19 slum areas reaching around 100000 people with a target population of 300000 people.• Planned, coordinated, promoted developing, edited content and summarised report outcomes workshops for world disability day event.• Built and maintain relationships with disability organisations and people with disability for providing aid, supplies and future awareness events.• Streamlined processes for effective functioning of the disability department at Chetanalaya.• Undertook written and design work including reports, articles and other relevant publications as needed topromote work of the organisation.• Identified and trained ‘champions’ within local disability communities and developed training programs forcoordinating and conducting research within the field.• Prepared grant proposal for new disability initiative in bordering states to create disability inclusive workenvironment.

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  Anthony Nolan

  • Laboratory Scientist

    • Jan 2013 - Sep 2015

    • Performed histocompatibility testing techniques for patient and donor matching. • Prepared medical questionnaires checks for first time donors to register onto the donor system. • Analysed data output and reported results to transplant centres. • Introduced annual reviewing and created new standard operating protocols (SOP).• Evaluated laboratory process quality, validated the process/regents and assisted with audits. • Gained an understanding of day-to-day running and maintenance of a pathology laboratory. • Lead the implementation of new stock check processing and ordering system in order to reduce costs and improve supplies.