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Job Description • Perform literature reviews and engage in scientific writing for manuscripts, articles, and book publications • Conduct research on relevant topics, gather data, and ensure compliance with proper procedures, policies, and health/safety guidelines. • Able to carry out research work independently and passion in research. • Manage patent and IP portfolios, including renewals and examinations. • Manage third-party outsourcing for laboratory testing and product safety assessments. • Serve as a regulatory liaison, managing documentation and submission processes for regulatory approvals. • Oversee preclinical studies, including managing quotations, payments, study progress, reporting, meeting coordination, and test item shipments, leading up to clinical trials. • Handle any other ad hoc projects assigned by the Company.