Clinical Trials Coordinator

Re:Cognition Health(RCH) is an international Company operating in the USA & UK. As a leading provider of clinical services specialising in cognitive impairment, RCH delivers expert clinical care to its patients. At the RCH’s first USA Center in Fairfax, N Virginia, this is delivered, primarily, through international Clinical Trials. RCH’s USA and UK centres are recognised as one of the pre-eminent global providers of Clinical Trials for progressive neurodegenerative diseases. In particular, for new generation medications for Alzheimer’s Disease. In 2018, Alzheimer’s was recognised by WHO, as a global pandemic.

Re:Cognition Health is accredited by the highest standard Global Clinical Trials accreditation in the UK and is currently seeking to ensure this same standard of accreditation underpins its USA operation. Essential to this endeavour is the requirement for all RCH staff to operate at the highest standards, adhering at all times to Re:Cognition Health’s own Standard Operating Procedures (SOP) and protocols, designated by the trial Sponsors and Clinical Research Organisations (CRO), with whom RCH contracts.

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 centre is safe, performance at CRA visits, external monitoring visits and FDA inspections is planned and executed for optimal success.

The post holder responsibilities include but are not limited to:

· 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 maximise business opportunities and recruit patients

· Adhere to the organisation’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 Centre is maintained and presented to the highest standards as expected by

· The organisation and that all equipment is calibrated and maintained in line with best practice

· To ensure adequate stock within the Centre 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 analyse 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

The Candidate
To be considered for the Clinical Trials Coordinator position, you will have the following education and experience:

· 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

The successful applicant will have access to all Re:Cognition Health’s benefits.

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

Job Type: Full-time

Salary: $65,000.00 - $75,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Ability to commute/relocate:

• Chicago, IL 60611 : Reliably commute or planning to relocate before starting work (Required)

Job Type: Full-time

Pay: $65,000.00 - $75,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Experience:

• Clinical Trials Coordinating: 3 years (Required)

Work Location: In person