Intern, Clinical Operations

Assist in identifying key process steps and corresponding key roles involved in the end-to-end process for either Clinical Study Conduct and/or Clinical Study Close-out. Assist with the translation of these process steps into corresponding documents such as Standard Operating Procedures (SOPs), Work Instructions (WI), Workflows, and managed layer documents. Participate in process meetings, assisting with meeting minutes and documentation of key points. Support project timelines, milestones, and communication. Working towards a bachelor's degree in health sciences Basic knowledge of drug development process Project/process management experience Strong written and verbal communication skills Attention to detail Proficient with MS Office Suite (Excel, Word and PowerPoint) General knowledge of process flows preferred Previous industry experience preferred Legal authorization to work in the U.S. At least 18 years of age prior to scheduled start date