Clinical Study Specialist - Contract - Basking Ridge, NJ
Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!
Proclinical is seeking a Clinical Study Specialist for a hybrid role based in the US. The Clinical Study Specialist provides technical and administrative support to the clinical study teams responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program.
Primary Responsibilities:
The successful candidate will receive assignments from the Clinical Study Lead or Clinical Study Associate Manager. They will be responsible for supporting both internally managed studies and those outsourced to Clinical Research Organizations (CROs).
In this role, a typical day might include the following:
This role might be for you if:
To be considered, a bachelor's degree with 2+ years of relevant pharmaceutical industry experience. In lieu of a bachelor's degree 5+ years of relevant pharmaceutical industry experience is required with a focus in clinical operations or trial management.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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