Join to apply for the Regulatory Affairs Associate III role at Katalyst CRO . Responsibilities include: Coordinate and prepare documents for regulatory submissions. Review and evaluate technical and scientific data for product submissions. Track the status and progress of regulatory documentation. Review, edit, and proofread regulatory documents. Assist in preparing labeling, SOPs, and departmental documents. Compile regulatory documents for submission under supervision. Participate as an active team member on project teams. Respond to regulatory authorities' questions. Maintain regulatory files according to requirements. Stay updated on regulatory requirements. Qualifications: Bachelor's degree or equivalent in pharmacy or related scientific discipline with 0-2 years of regulatory experience, preferably in healthcare. Strong scientific knowledge and communication skills. Proficiency in systems such as word processing, spreadsheets, databases, and online research. Ability to multitask, prioritize, and contribute to multiple projects. Additional details: Seniority level: Entry level Employment type: Full-time Job function: Legal This job posting appears active; no indication of expiration. #J-18808-Ljbffr Katalyst CRO
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