Senior Medical Scientist

vor 3 Wochen


City of Melbourne, Österreich WorkTrybe Vollzeit

Join to apply for the Senior Medical Scientist role at WorkTrybe 4 days ago Be among the first 25 applicants Join to apply for the Senior Medical Scientist role at WorkTrybe You’ll play a key role in the development, safety, and regulatory compliance of new therapies. Working cross-functionally with Clinical Development, Regulatory Affairs, and Pharmacovigilance teams, you’ll help ensure scientific excellence across every stage of the process. What You’ll Do As a Senior Medical Scientist, you’ll contribute your expertise to ensure product safety, regulatory compliance, and scientific integrity across all programs. Key Responsibilities Provide scientific and medical expertise during the design, execution, and analysis of clinical trials. Review study protocols, clinical study reports, and safety documentation. Collaborate with regulatory teams to prepare and review INDs, NDAs, and CTAs. Respond to regulatory authority queries and ensure compliance with global standards. Assess adverse event reports and contribute to safety signal evaluations with the Pharmacovigilance team. Participate in Data Monitoring Committees (DMCs) and support safety review processes. Develop and review publications, presentations, and educational materials aligned with corporate strategy. Deliver internal training on clinical and scientific topics to ensure consistent and compliant communication. Partner with Clinical Operations, Regulatory Affairs, and Commercial teams to align on development and market access strategies. Maintain ethical standards and ensure all materials and activities meet regulatory and scientific requirements. About You MD, MD/PhD or PhD in a relevant field (e.g. pain, musculoskeletal disease, immunology). Minimum 5 years’ experience in clinical research and development. 3-5 years’ experience in the pharmaceutical or biopharmaceutical industry. Strong understanding of clinical trial and safety oversight processes. Excellent communication, collaboration, and organisational skills. The Benefits Scientifically rigorous: You take pride in high-quality data, critical thinking, and evidence-based decision-making. Agile and collaborative: You value clear communication, teamwork, and adaptability in a fast-moving environment. Impact-driven: You’re motivated by the opportunity to translate science into meaningful therapies that change lives. Accountable and transparent: You own your work, follow through on commitments, and uphold the highest ethical standards. Innovative yet disciplined: You embrace new ideas while maintaining the structure and compliance essential to successful global trials. You’ll be part of a close-knit team working toward something bigger — bringing hope, science, and new possibilities to patients worldwide. NEXT STEPS Please apply via the link or email to arrange a confidential discussion. Seniority level Mid-Senior level Employment type Full-time Job function Science, Product Management, and Research Industries Pharmaceutical Manufacturing #J-18808-Ljbffr



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