Job Description

Compass Life Sciences are delighted 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

Senior 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

To be considered for this role, the ideal candidate will have the following:

Essential:
Life sciences degree or similar with a minimum 2:1

At least 2 years experience as a Clinical Trials Coordinator

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

In exchange for this our client is offering the following:
Competitive salary

Progression opportunities

Private health

Life insurance

Pension scheme

Additional soft benefits

Contact

If you would like to be considered for this position, contact Matteo Berogna directly on direct line: 02394 214480 or mobile number: 07774314025. Alternatively email an updated CV to mberogna@compassltd.co.uk .

Recommendations

Not for you but know someone who would be interested? Compass Associates Ltd. trading as Compass Life Sciences are acting as a Recruitment Consultancy for this permanent vacancy; we offer up to £200 worth of John Lewis or Amazon Vouchers should we successfully place someone you recommend.

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