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This is a company which has been established for over 20 years and is recognised as one of the top 10 CRO’s through their innovative style and strong focus on the quality of their work. As an organisation that has a strong presence in over 40 countries, they are truly global and are involved in some of the most cutting edge clinical studies. With a clear route for career progression within their organisation and the opportunity to be involved in mentoring and leadership activities, this dynamic company have a passion for developing individuals and is looking for those individuals who strive to achieve.
Working as a CRA (CRA I) within this established organisation, you will be given the autonomy to conduct full site monitoring on various Phase I-IV studies. Working alongside senior CRA’s and Lead CRA’s you will be in a position to quickly learn and progress through the company. Responsibilities that you will have are:
· Performing site monitoring activities
· Site interactions – investigator/Sponsors
· Closely liaise with Senior CRA’s
This would be an ideal opportunity for a Clinical research associate, CRA who is driven to expand on their experience within a biotech or pharmaceutical company to really progress in their career.
· Experience in France site monitoring activities and site coordination
· In depth knowledge of GCP practices within a biotechnology, pharmaceutical or CRO company.
· Minimum of a degree in Life Sciences.
· Fluent in English and French.
Salary per annum: €30,000- €35,000
To discuss this opportunity in more depth and for a full job description, apply below to be contacted; no CV is submitted until a full discussion has taken place.
This position is being handled by Kavita Najran, Meet, 0044 (0) 781 4180 900
Find out more about meet at www.peoplewithchemistry.com
Associated keywords: CRA, Clinical research associate, clinical trials, CRA I, monitoring, development, CRO, global international, field based, home based, France