Clinical Trials Coordinator in Chicago, Illinois at Re.Cognition Health US

ABOUT RE:COGNITION HEALTH

Re:Cognition Health is a pioneering brain and mind clinic that specializes in the treatment and care of people showing symptoms of cognitive impairment. Utilizing the latest progressive medical research and evidence-based treatments, we are passionate about transforming and optimizing cognitive performance through education, clinical excellence and by providing access to emerging treatments.

We value people who are dedicated, hardworking and looking to contribute to the growth of our business at an exciting time. Our vision is to become the recognized worldwide leader in the diagnosis, treatment and care management of individuals experiencing cognitive impairment. Come join our team where everyone is valued and where critical and important work is being done!

To find out more about our company, please visit https://recognitionhealth.com

About the role

• The post holder will be held accountable to the Senior Clinical Trials Coordinator (Chicago) for the highest standards of operational delivery of the Clinical Trials for which the post holder is appointed to co-ordinate. This includes responsibility for delivering these trials according to clinical trials “Good Clinical Practice” (GCP), ensuring appropriate resources, including professional skill mix, training and competency are in place at all times. Practice at the center is safe, performance at CRA visits, external monitoring visits and FDA inspections is planned and executed for optimal success.

What you'll do

• To ensure that the highest levels of customer/patient care and clinical delivery are maintained at all times
• To support the development of the business by working closely with clinicians and consultants to maximize business opportunities and recruit patients
• Adhere to the organization’s policies and SOPs and ensure all members of the clinical trials team are trained and compliant
• To ensure that all administration is performed accurately and in a timely way including the entry of patient records on all necessary databases and forms
• To ensure that all patient records are accurate, stored appropriately and all confidential information is retained in accordance with data protection requirements
• To ensure that the Center is maintained and presented to the highest standards as expected by
• The organization and that all equipment is calibrated and maintained in line with best practice
• To ensure adequate stock within the Center ensuring that it is ordered in a timely way and that stock is controlled
• To seek feedback from patients as to their experience and record these findings and analyze them to support the ongoing development of the service
• To be responsible for answering all queries and SAE and related IRB/FDA reporting within the time frames dictated for each study and GCP

Qualifications

• 5 years experience in Clinical Trials Coordination, operation, set-up and delivery.
• Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint)
• Experience with electronic data capture (EDC) systems