Senior Medical Scientist

1 day ago

Melbourne, Victoria, Australia WorkTrybe Full time $120,000 - $180,000 per year

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 to arrange a confidential discussion.

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