An expanding CRO have an exciting opportunity for a Senior Clinical Research Associate to join the team. This position offer the opportunity to undertake project management responsibilities alongside the CRA role. It is a remote opportunity for the foreseeable future and offers a salary reflective of the responsibilities.
The fast-growing CRO have over two decades worth of experience which have allowed them to develop trusted relationships with clients around the world, ensuring they are first choice in the conducting of their clinical trials. There is a continued emphasis on maintaining client relationships by understanding the different needs and objectives these sponsors may have, and tailoring each trial as necessary to achieve optimum results.
The Senior CRA Position
This is a position within a fast-paced environment, where there is a chance to continue to develop your clinical skills and really make a difference. The key responsibilities are to identify, select, initiate and close-out investigational sites for a wide range of clinical trials.
Further responsibilities include –
Communicate effectively with investigators and other research personnel, maintaining a professional demeanour.
Review source documentation to confirm subject eligibility for the clinical trial and to confirm that the correct informed consent process has been followed.
Complete project activities associated with monitoring functions of clinical research studies whilst developing mastery and a thorough understanding of the drug development process.
Senior CRA Requirements.
5 years monitoring experience is essential.
Preference for oncology experience.
Strong academic life science background.
If this sounds like the role for you, please apply now
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