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The Role
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
We’re in an exciting growth phase — advancing our late-stage (Phase III) clinical programs — which means your work will have real and immediate impact. You’ll thrive with our client if you enjoy working in an environment that is:

• 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 kylie.saunders@worktrybe.com to arrange a confidential discussion.

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