My client, a Medical equipment manufacturer has a requirement for a Clinical Research Associate to join their business on a permanent, remote working basis.
As Clinical Research Associate, you will conduct the full monitoring cycle of pre-study, site qualification, initiation visits, routine monitoring and close out visits. Preparing reports and ensure investigator site files are maintained accurately at each site.
As CRA, you will be home based with travel throughout the UK and will be required to attend our Leeds based site at least once a month for key stakeholder meetings. You will assist with identifying clinical sites, assisting the Clinical Project Manager to prepare clinical investigation plans and reports and reviewing CRF specifications.
To be considered for the role of Clinical research Associate, you will:
- Have experience within the Medical Device/ IVD industry
- Have worked in a similar / relevant Clinical research position
- Preparing clinical investigation experience
- Educated to a degree level
- Be flexible with travel to key sites
- Strong autonomous work ethic
This is an great opportunity with varied duties for career progression in a well established company. This is a permanent role.
Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.