Scientific Leader

6 days ago

Melbourne, Victoria, Australia beBeeClinical Full time $150,000 - $200,000

Medical Director Opportunity

We are seeking an experienced and hands-on Medical Director to join a dynamic, science-driven team leading the charge in immuno-oncology research.

  • Ground-breaking Science: Product is first-in-class with impressive survival data in solid tumours. Opportunity to lead a clinical program with high unmet need.
  • Clinical Momentum: Strong feedback from ASCO presentations, robust interest from investigators, and clear differentiation in a space with few competitors.
  • High-Impact Role: Lead the clinical strategy in a pivotal trial, with support from a seasoned Chief Medical Officer and a high-performing biotech team.
  • Agile Culture: Flat structure, collaborative ethos, flexible working arrangements, and a genuine passion to improve patient outcomes.
Job Description

You will provide medical oversight for clinical trials, develop clinical study documents, engage with clinical sites and investigators, partner with pharmacovigilance providers, collaborate with Clinical Operations, support regulatory strategy, lead the medical review of data, prepare and present data, draft manuscripts for peer-reviewed journals, and contribute to medical strategy.

  • Reporting to the CMO, and working closely with internal teams and external partners (CROs, sites, KOLs).
  • Providing medical oversight for clinical trials for the upcoming Australia-based Phase IIb study.
  • Leading or supporting the development of clinical study documents, including synopses, protocols, ICFs, investigator brochures, and clinical sections of regulatory submissions.
  • Engaging directly with clinical sites and investigators, answering protocol questions and supporting patient enrolment and eligibility assessment.
  • Partnering with pharmacovigilance providers to assess safety events, determine reportability, review MedWatch reports, and prepare DSURs.
  • Collaborating with Clinical Operations to ensure optimal study set-up and delivery.
  • Supporting regulatory strategy with interface across R&D, CMC, and external stakeholders.
  • Preparing and presenting data to internal stakeholders, safety monitoring committees, and at scientific conferences.
  • Drafting manuscripts for peer-reviewed journals to disseminate key clinical findings.
About You

We are looking for a Medical Director with a medical degree, significant experience in clinical development, and strong knowledge of clinical trial processes, GCP, and global regulatory requirements.

  • Australia, Victoria.
  • Experience in protocol authorship and regulatory submissions.
  • Exceptional communication and presentation skills.
  • Demonstrated ability to work cross-functionally and manage external partners.

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