Assist in delivering studies to support product development, manufacturing, and post-market surveillance for all ADC products. Maintain, calibrate, and use laboratory equipment; perform site visits to support and train on equipment. Ensure adequate stock, accountability, and shipment of study materials. Assist CRAs in preparing and maintaining study documentation and files and facilitate archiving of in-house study documentation. Maintain effective communication with study centres, external partners, and ADC internal groups to ensure successful study implementation. Ensure clinical studies are conducted according to health and safety guidelines and dispose of study materials appropriately. Review clinical study requests, provide clinical input, and liaise with project teams to meet clinical testing needs. Maintain the effectiveness of the Quality System in accordance with divisional and corporate requirements and applicable regulations. Identify and implement changes to clinical processes and procedural documentation. Ensure all clinical studies meet internal/external standards and GCP requirements. Adhere to EHS regulations and Abbott standards, being accountable for the Health & Safety of yourself and others. Qualifications:
A levels or equivalent. Must be accurate and organized with good attention to detail. Good judgment and communication skills for interaction with study site personnel and external vendors. Ability to prioritize work in a complex environment, with strong analytical skills to digest information from clinical studies and report findings. In addition to a competitive salary, Abbott offers a highly attractive benefits package which includes a defined-contribution pension scheme, a share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme which you can tailor to your own requirements.
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