Industry
临床研究患者安全CRO药物开发
Description
As an Intern in Patient Safety Solutions, you will support the global patient safety team in ensuring the highest standards of safety monitoring and reporting for clinical trials.
Your responsibilities will include:
Assisting in the collection, processing, and documentation of adverse event (AE) and serious adverse event (SAE) reports from clinical trial sites.
Performing initial review and data entry of safety data into the safety database, ensuring accuracy and compliance with regulatory requirements.
Requirements
Qualifications and requirements:
Currently enrolled in a Bachelor's or Master's degree program in life sciences, pharmacy, nursing, or a related field.
Strong attention to detail and organizational skills.
Excellent written and verbal communication skills in English.
Want to know more?
Scan QR code to add WeChat Work for personalized position consultation

Office Hours: Mon-Fri 9:00-18:00
Position Info
- Category
- internship
- Location
- 巴西 · Estado de São Paulo