Preclinical Research Associate

Job Summary

Providing critical support for regulatory submissions, the full-time Preclinical Research Associate will perform quality control reviews, manage document formatting, and assist with Veeva document lifecycle management in a remote capacity.

Key responsibilities

• Conduct quality control reviews of nonclinical content for DMPK and Toxicology reports
• Edit and format regulatory submission documents to ensure compliance with style guides and guidelines
• Support literature reference activities, including retrieval and upload to electronic document management systems

Required qualifications

• Bachelor's degree in Life Sciences with 3 to 4+ years of relevant experience
• In-depth knowledge of Good Laboratory Practices, FDA regulations, and ICH guidelines
• Proven ability to manage multiple projects in a fast-paced environment
• Proficiency in Microsoft Suite; experience with Veeva preferred
• Experience with regulatory submissions is a plus