- You will ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions).
- A degree in Life Science or equivalent experience;
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clinical study coordinator - lecce - beBeeCRA
Titolo del lavoro: Clinical Research Associate I/ Clinical Research Associate II
Descrizione
Clinical Research Associate Opportunity
Precision for Medicine is a cutting-edge CRO that combines innovative technologies, expertise and operational scale to accelerate the development of life-changing therapies.
About the Role:
We are seeking an experienced Clinical Research Associate to join our team in Italy. As a key member of our site management group, you will be responsible for monitoring and owning the progress of clinical studies at investigative sites.
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Preliminary Requirements:
Tech Specs:
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Glacier Monitoring Assistant
Solo per membri registrati Lecce, Apulia
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ELI - Stage Structure Dept
A tempo pieno Solo per membri registrati Brindisi
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ENVIRONMENTAL AFFAIRS OFFICER
Solo per membri registrati Brindisi
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ENVIRONMENTAL AFFAIRS OFFICER
Solo per membri registrati Brindisi, Puglia
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ENVIRONMENTAL AFFAIRS OFFICER
Solo per membri registrati Brindisi, Apulia