Join Abbott as a Clinical Study Coordinator in Witney!
Are you passionate about clinical research and looking to make a significant impact? Abbott, a global healthcare leader, is seeking a Clinical Study Coordinator to join our team in Witney, UK.
Abbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.
Abbott Diabetes Care designs, develops, and manufactures leading-edge blood glucose monitoring technology for use in both home and hospital settings, including our revolutionary Freestyle Libre Flash Glucose Monitoring System.
In our Centre of Excellence in Witney, we design, develop and manufacture test strips and biosensors which are used by patients and healthcare professionals for the day-to-day management of diabetes.
As a result of strong business growth, industry-leading product development in the biosensor business and a long-term commitment to manufacturing and innovation in our Witney Centre of Excellence, we have a fantastic opportunity for a Clinical Study Coordinator to join our expanding highly skilled team.
Your Role:
As a Clinical Study Coordinator, you will:
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. #J-18808-Ljbffr
Are you passionate about clinical research and looking to make a significant impact? Abbott, a global healthcare leader, is seeking a Clinical Study Coordinator to join our team in Witney, UK.
Abbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.
Abbott Diabetes Care designs, develops, and manufactures leading-edge blood glucose monitoring technology for use in both home and hospital settings, including our revolutionary Freestyle Libre Flash Glucose Monitoring System.
In our Centre of Excellence in Witney, we design, develop and manufacture test strips and biosensors which are used by patients and healthcare professionals for the day-to-day management of diabetes.
As a result of strong business growth, industry-leading product development in the biosensor business and a long-term commitment to manufacturing and innovation in our Witney Centre of Excellence, we have a fantastic opportunity for a Clinical Study Coordinator to join our expanding highly skilled team.
Your Role:
As a Clinical Study Coordinator, you will:
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. #J-18808-Ljbffr
