<img alt="" src="https://secure.smartenterprisewisdom.com/780275.png" style="display:none;">
Back to All Jobs...

Clinical Trials Coordinator – CRO - Plymouth – Up to £30,000 Salary DoE + Benefits


The Company

  • An emerging CRO, specialising in treatment for mental health services. Working with clinical trials such as Migraine, ADHD, Dementia and Brain Injuries.

  • A presence in the UK and the US, looking to grow in both locations.

The Role

  • 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


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

  • At least 1-year experience within clinical trials research at clinical trials coordinator level or equivalent.

  • Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint).

  • Experience with electronic data capture (EDC) systems.

  • Ideally experience with cognitive clinical trials.

What should you do next?

A guaranteed development opportunity for somebody looking to grow their career within the clinical trials field, focusing on neuroscience specialities, an ever growing therapeutic area in the world of research.

To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments, we can make to assist you at interview then please let us know and we'll be more than happy to assist.


Apply Now!

Job Consultant

Amie Lovelock

Clinical Research

Recruitment Consultant

+44 (0) 2393 874 293



Related Jobs

Clinical Research

Regional General Manager - Reproductive Healthcare

Permanent ,
Clinical Research

Research Nurse – Leading CRO

Permanent ,
Clinical Research

Junior Colorectal Nurse – Leading wound care manufacturer

Permanent From £31000 ,

Get The Resources You Need In The Candidate Hub