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- Tasks: Support Clinical Research Associates in coordinating clinical studies and managing product logistics.
- Company: Abbott Diabetes Care is a leader in glucose monitoring technology, improving lives globally for over 135 years.
- Benefits: Enjoy a competitive salary, flexible benefits, private healthcare, and unique wellness initiatives like yoga and bee keeping.
- Why this job: Join a dynamic team making a real impact in diabetes care with opportunities for professional growth and innovation.
- Qualifications: Secondary level education with an interest in Science, Technology, and clinical trials; strong communication and organisational skills required.
- Other info: Collaborate with multiple teams and work in a fast-paced, evolving environment.
The predicted salary is between 28800 - 43200 £ per year.
Known for the development of revolutionary technologies, Abbott Diabetes Care (ADC) designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings. We are passionate about doing work that improves the quality of people\’s lives. We now have an exciting opportunity in our growing Clinical Affairs function for a Clinical Study Coordinator.
The Clinical Study Co-coordinator assists delivery of studies to support both product development, manufacturing and the post market surveillance program for all ADC products
ABOUT YOU:
In this role, you will typically find yourself supporting the Clinical Research Associates (CRAs) in their study activity. This covers various activities, including ensuring adequate stock levels of product; scheduling, prioritising and coordinating shipment of product to trial sites; decontaminating returned product; assisting in preparation and maintenance of documentation and files; and liaison with both internal and external stakeholders to ensure smooth running of trial activities.
To be successful, you will ideally be qualified to secondary level education, and have an interest in Science, Technology, and clinical trials. The ideal candidate will be a proactive individual who takes initiative and is able to work within a team. You will need to be organised, and have good communication and time management skills, and be comfortable working in a fast-paced, changing environment. There will be opportunity to collaborate with multiple teams across the Abbott Diabetes Care business, including Data Management, Regulatory, Statistics, and Scientific Affairs.
Abbott is about the power of health. For more than 135 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.
World Leader in Glucose Monitoring, Abbott Diabetes Care designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings. We have a Centre of Excellence in Witney for the development and manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. The site has been instrumental in the research, development and manufacture of the FreeStyle Libre Flash Glucose Monitoring System as well as exciting developments in the Libre family including FreeStyle Libre 2, FreeStyle Libre 3 and the Libre Sense system. We are passionate about doing work that improves the quality of people\’s lives.
At Abbott, you will be part of a dynamic team that is making a real difference in diabetes care. You will have the opportunity to work on cutting-edge technology and contribute to innovative solutions that improve lives. We offer a collaborative work environment, opportunities for professional growth, and the chance to be part of a company that values scientific excellence and innovation.
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. We like to help our employee\’s live life to the fullest, and therefore we offer a range of optional initiatives for you to get involved in, including onsite allotments, couch to 5k campaigns, bee keeping, yoga and more!
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Clinical Study Coordinator employer: Abbott
Contact Detail:
Abbott Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Coordinator
✨Tip Number 1
Familiarise yourself with the latest trends in glucose monitoring technology. Understanding the products and innovations at Abbott Diabetes Care will not only help you during interviews but also show your genuine interest in the role.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have experience with diabetes care. Engaging with them on platforms like LinkedIn can provide insights into the role and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss your organisational and time management skills in detail. Think of specific examples from your past experiences where you successfully managed multiple tasks or projects simultaneously.
✨Tip Number 4
Research Abbott's values and mission, particularly their commitment to improving health. Being able to articulate how your personal values align with theirs can make a strong impression during the interview process.
We think you need these skills to ace Clinical Study Coordinator
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Clinical Study Coordinator position at Abbott Diabetes Care. Understand the key responsibilities and required skills, such as supporting Clinical Research Associates and managing trial logistics.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job requirements. Emphasise your organisational abilities, communication skills, and any previous experience in clinical trials or related fields.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for science and technology, as well as your proactive nature. Mention specific examples of how you have successfully managed projects or collaborated with teams in fast-paced environments.
Highlight Relevant Qualifications: If you have any qualifications or certifications related to clinical research or healthcare, be sure to mention them in your application. This could include coursework, training, or relevant volunteer experiences that demonstrate your commitment to the field.
How to prepare for a job interview at Abbott
✨Show Your Passion for Healthcare
Make sure to express your enthusiasm for improving people's lives through healthcare. Discuss any relevant experiences or projects that demonstrate your commitment to the field, especially in relation to diabetes care and clinical trials.
✨Highlight Your Organisational Skills
As a Clinical Study Coordinator, being organised is key. Prepare examples of how you've successfully managed multiple tasks or projects simultaneously, and be ready to discuss your time management strategies during the interview.
✨Demonstrate Team Collaboration
Since this role involves liaising with various teams, share specific instances where you've worked effectively within a team. Highlight your communication skills and how you’ve contributed to achieving common goals.
✨Prepare for Technical Questions
Brush up on your knowledge of clinical trials, glucose monitoring systems, and related technologies. Be prepared to answer questions about the processes involved in clinical studies and how you can support CRAs effectively.
