Clinical Trials Coordinator

1 week ago

Winchester, United Kingdom Compass Life Sciences Full time

Compass Life Sciences are privileged to be partnering with an emerging CRO, specialising in treatment for mental health services. Working with clinical trials such as Migraine, ADHD, Dementia and Brain Injuries, supporting in their search to appoint a Clinical Trials Coordinator.

**Responsibilities**:
Clinical Trials Coordinator responsibilities will include but are not limited to:
Accountable for ICH-GCP compliance across all assigned studies
To ensure that the highest levels of customer/patient care and clinical delivery are always maintained
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 complete the necessary start-up activities including assisting the Clinical Trials Start Up Specialist with any completion and submission of Non-NHS SSI forms to the relevant REC for new studies to be conducted at the Centre as and when required
To perform internal audits of working practices within the Centre to measure compliance against company SOPs and GCP as and when required

**Requirements**:
**Essential**:
Life sciences degree or similar with a minimum 2:1
At least 1-year experience within clinical trials research
Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint)
Experience with electronic data capture (EDC) systems

**Desirable**:
Ideally experiences with cognitive clinical trials
Ideally previous experience as a Clinical Trials Coordinator in a similar field within the private health sector

**In exchange for this our client is offering the following**:
Competitive salary
Progression opportunities
Private health
Life insurance
Pension scheme
Additional soft benefits

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