As a Clinical Research Associate II/Senior Clinical Research Associate, you will monitor clinical trials, ensuring compliance with protocols and regulatory requirements. Responsibilities include site management, data collection, and reporting.
A Bachelor's degree in Life Sciences or related field, with at least 3 years of experience in clinical research. Strong knowledge of GCP guidelines, excellent communication skills, and the ability to work independently are essential.
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A precision medicine contract research organization (CRO) offering integrated services to support the development of novel compounds in oncology and other therapeutic areas.
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