Clinical Trials Coordinator - Permanent - Winchester

Maxxima are working with the leading provider of clinical services specialising in cognitive impairment. We are currently looking for an experienced Clinical Trials Coordinator. This post is based in Winchester, Hampshire a lovely part of the UK, which is on the edge of England's South Downs National Park.
About the role:

As Clinical Trials Coordinator you will be responsible for the set up and delivery of all clinical trials according to RCH governance, operational, financial and developmental strategies and in compliance with Good Clinic Practice (GCP) principles.

What’s in it for you as a Clinical Trials Coordinator:

• £30’000-£36’000 per annum + Benefits
• The opportunity to gain maximise business opportunities and recruit patients

Your main responsibilities as Clinical Trials Coordinator:

• Assist in the preparation for any Sponsor, CRO and regulatory audits and inspections
• Assist The management of the clinical trials’ operational aspect including clinical trials participants and any external vendors
• Be accountable for ICH-GCP compliance across all assigned studies

What we are looking for in a Clinical Trials Coordinator:

• Life sciences degree or similar with min 2:1
• Minimum of 2 years’ experience working as a CTA/Senior CTA or CTC are essential
• Experience with electronic data capture (EDC) systems

Next steps:

If you are interested to hear more, either hit the APPLY NOW button or reach out to Charlotte on 02033986694 or charlotte.oliver@maxximagroup.com