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.
申请条件
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.
雇主简介
Fortrea is a global contract research organization (CRO) providing clinical development and data management services to the pharmaceutical, biotechnology, and medical device industries.