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| Job Location | Motherwell |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Clinical Research AssociateMotherwell32 Days Holiday + Overtime + Pension + Training + ProgressionExcellent opportunity for a Clinical Research Associate to join an expanding, growing company offering long term career progression and possibilities to move into senior and management roles within the company.On offer is a varied and interesting position working with leading companies in the industry.This company, who specialise in Life Science industry, have big plans in place to continue their expansion over the coming years. They currently work with many companies across the south of the UK and have 5 global locationsIn this role, the successful candidate will be responsible for the performing site start up procedures, routine monitoring and site closure. As well as the ability to manage multiple priorities across various clinical trialsThis is a fantastic opportunity to join a company with big plans in place to grow and expand in the future in an cutting edge and flexible working environment.THE ROLE*Working in a small team on Covid 19 Virus treatments.*Reporting directly to Clinical Operations ManagerTHE PERSON:*Monitoring experience*Oncology/Viral experience beneficial *Relevant degree in scientific discipline is beneficialRTR95493To apply for this role or for to be considered for further roles, please click "Apply Now" or contact Tom Bartley at Rise Technical Recruitment.This vacancy is being advertised by Rise Technical Recruitment Ltd. The services of Rise Technical Recruitment Ltd are that of an Employment Agency.Rise Technical Recruitment Ltd regrets to inform that our client can only accept applications from engineering candidates who have a valid legal permit or right to work in the United Kingdom. Potential candidates who do not have this right or permit, or are pending an application to obtain this right or permit should not apply as your details will not be processed. Required skills
Keyskills :
In this role the successful candidate will be responsible f the perfming site start up procedures routine moniting and site closure. As well as the ability to manage multiple priities across various clinical trials