Found Description
Join bioLytical as a Clinical Research Associate, where you'll support innovative clinical studies and require frequent travel to various sites. Your skills in data management and compliance will make a significant impact.
In this role, you will work closely with the Vice President of Compliance and be responsible for the development and oversight of trial protocols. This includes conducting data analysis, ensuring compliance with industry standards, and training clinical staff. You’ll travel around 50% of the time to ensure ongoing support at study sites worldwide.
Key Responsibilities:
• Create trial protocols and submit ethics applications
• Generate scientific reports and regulatory documentation
• Monitor site activities and ensure adherence to protocols
• Train site personnel on bioLytical products and compliance
• Oversee inventory and document investigational product dispensing
Requirements:
• Bachelor’s degree in Biological Science or related field
In this role, you will work closely with the Vice President of Compliance and be responsible for the development and oversight of trial protocols. This includes conducting data analysis, ensuring compliance with industry standards, and training clinical staff. You’ll travel around 50% of the time to ensure ongoing support at study sites worldwide.
Key Responsibilities:
• Create trial protocols and submit ethics applications
• Generate scientific reports and regulatory documentation
• Monitor site activities and ensure adherence to protocols
• Train site personnel on bioLytical products and compliance
• Oversee inventory and document investigational product dispensing
Requirements:
• Bachelor’s degree in Biological Science or related field
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