Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $18 billion and approximately 55,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient ...
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The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and Sponsor’s SOPs. The CRA conducts site visits to assess protocol and regulatory compliance and manages required documentation and ensures that data will pass international quality assurance audits. They also develop collaborative relationships with investigational sites. You will be fully integrated into the client's systems, using their SOPs.
Education and Experience:
Medical, pharmaceutical or other life-science related degree
At least 1 year of independent monitoring experience in a CRO, pharmaceutical or biotech company
Additional Requirements:
Demonstrated clinical trial monitoring skills
In-depth understanding of ICH/GCP guidelines
Excellent standard of verbal and written communication skills in English
Highly organized with strong attention to detail and deadlines
Advanced skills across all of the Microsoft packages
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