Harmony Ogbusi

Experience

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  661 Nigeria Airforce Hospital ikeja Lagos

  Mar 2017 - Sept 2017

  Industrial Trainee

  • Partook in clinical ward rounds with the Officer Commanding (OC) Pharmacist to assess and provide the health needs of admitted patients.• Assisted the OC Pharmacist in disinfection and sterilization of medication compounding equipment.• Engaged in clinical patient follow up for discharged patients who are missing a particular medication collection cycle.

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  Brightmex Pharmacy Nig ltd

  Sept 2018 - Oct 2021

  Senior Pharmacist
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  AFRAB CHEM

  Jan 2019 - Feb 2020

  Production Pharmacist

  • Exploration of different standard operating procedures in line with the current Good• Carrying out Batch Manufacturing Record (BMR) in line with cGMP• Supervision of the dispensation of pharmaceutical raw materials for manufacture.• Participated in the production activities of medicines of differing dosage forms namely;o Tabletso Liquidso External preparations• Effectively worked with the management to prioritise tasks and organise workflow toincrease efficiency.• Assessing process risks and identifying process deviations as regards quality management. • Participation in new plant design to aid drug production flow while ensuring cGMP• Raw material procurement, storage and monitoring. Show less

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  Health Quaters pharmacy and stores

  Oct 2019 - Aug 2021

  Pharmacist
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  Irenecare international limited

  Aug 2020 - Feb 2021

  Pharmacist
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  Turmeric pharmacy

  Feb 2021 - Jul 2021

  Pharmacist
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  The Royal Marsden NHS Foundation Trust

  Dec 2021 - Jul 2023

  -Management and maintenance of clinical trial documents such as Patient Information Sheet housing the Tissue for Future Research consent forms.-Providing assistance in the review of trial documents such as processing guidance documents,laboratory manuals and SOPs.-Maintenance and management of all equipment used by various trial teams to facilitate specimen processing and storage.-Assisted in the provision of laboratory skills training to new and returning staff members when necessary.-Coordinated the archiving of trial documents held in the custody of the trust's biobank.-Ensure all tissue data collection and processing adheres to the ethical guidelines for specimen collection as adopted by the trust.-Order, receive, manage and provide account for trial supplies/stock. Show less At the Head, Neck and Thyroid Oncology Department, my core responsibilities are;• To ensure that all work is carried out in line with laboratory Manuals, protocols, Standard Operational Procedures and Departmental and National Policies (e.g The Human Tissue Act)• To see that tissues are stored at -80oC or snap freezed with liquid nitrogen as required.• To see to the accurate labeling and processing of samples in line with stipulated guidelines.• To ship samples, as ambient or using dry ice as requested via external courier services.• To work semi-independently across both trust sites(Chelsea and Sutton) to ensure timely collection of samples for use by theresearch team.• To liaise with scientists and clinicians between the RMHNHST and the Institute of Cancer Research• To liaise closely and coordinate tissue collection and data collection with the Clinical ResearchNurses, the Histopathology departments of the RMNHST and the ICR and other members of thehead, neck and thyroid clinical trials unit.• To coordinate the dispatch of samples to other centres as specified by trial protocols• To keep and continuously update accurate databases containing information relating to the collected tissues and stored samples.• To ensure that all tissue and data collection adheres to current ethical guidelines for tissue collection adopted by the RMHNHST.• To maintain adequate stocks of all reagents and consumables through the timely ordering of supplies.• To request samples for the unit nationally and internationally and coordinate the receipt of these samples in a timely fashion and in accordance with the regulations.• To maintain accurate logs of samples, and paper trails of the movement of pathological samples in and out of the RMHNHST.• To prepare, participate and/or lead any potential internal and/or external regulatory audits and statutory inspections.• To assist in developing service plans for the RMHNHST Tissue Collection Facility when requested. Show less At the West Wing Lab., my responsibilities were;•Tissues samples reception, processing [including accurate aliquoting and labelling] from various tumor groups (Head and Neck, Breast, Prostate, Neuro-Oncology, hematology, Gynecology, Gastrointestinal and Lymphoma, Urology, Lung and the Institute of Cancer Research).• Implementing laboratory procedures for the recording of samples, processing and shipment, according to laboratory protocol and ensuring barcoding of samples is correctly implemented at all stages of the procedures. Using Freezer Pro and T drive, to assist with the retrieval of data for audit and query purposes when requested.•Setting up of trial log from different World Contract Research Organizations like the PPD, Labcorp, Cerba Research, Q-squared solution etc., for both new and amended trial protocols for the west wing laboratory.•Carrying out routine housekeeping tasks including lab stock checking, ordering lab materials, preparing buffers, aliquoting reagents, waste management, looking after communal equipment and facilities.•Co-ordinate the shipments of processed human tissue samples, either ambient or frozen, depending on their shipment guidelines. •Assist in the routine maintenance of the laboratory equipment (like centrifuges andfreezers on a regular basis) as designated by monitoring safety, performance, calibration and temperature as stipulated by he SOPs.•Participating in continuing professional development, taking measures to acquire, improve and apply scientific/technical skills by relevant training or meetings.•Support the Laboratory Manager on Corrective and Preventive Actions (CAPAs) related to sample processing, data recording, sample shipments and protocol amendment.•Assist in the training of new laboratory staff of the West Wing Clinical Research Centre in accordance with the stipulated SOPs and cGCP.• To attend site initiation visits in absence of laboratory manager and feed back to the team any issues identified. Show less

  • Biobank Specimen Coordinator

    Mar 2023 - Jul 2023

  • Biological Specimen Coordinator

    Nov 2022 - Feb 2023

  • Medical Laboratory Assistant

    Dec 2021 - Oct 2022
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  King's College London

  Aug 2023 - Apr 2024

  Clinical Trials Senior Specialist Technician