Multi-tasking Research Associate with 5+ years of pharmaceutical Research & Development experience. Outgoing, organized, and detailed oriented. Execution of protocol writing & development, GLP/GMP/FDA and other regulatory documentation as well as biological and chemical data analysis while meeting strict deadlines. Knowledge of FDA animal research guidelines and initiation of all aspects of animal studies with experimental compounds. Proficient with Microsoft Office, excellent time management, and data analysis. Collaborative leader with dedication to partnering with coworkers to promote engaged, empowering work culture. Documented strengths in building and maintaining relationships with diverse range of stakeholders in dynamic, fast-paced settings.
Identified opportunities to streamline processes and improve office operations and efficiency.