Overview
- ASX-listed oncology drug development company advancing Phase 3 and Phase 1 clinical programs
- Full-time position with flexible/work-from-home environment and competitive remuneration package
- Clinical development role with strong focus on investigator engagement, advisory boards, and trial execution
About Racura Oncology
Racura Oncology (ASX: RAC) is a Phase 3 clinical-stage biopharmaceutical company with a mission to silence cancer. Racura is advancing a proprietary formulation of (E,E)-bisantrene (RC220) to address the high unmet needs of patients across multiple oncology indications, with a Phase 3 clinical program in acute myeloid leukaemia (AML), a Phase 1 program in mutant epidermal growth factor receptor non-small cell lung cancer (EGFRm NSCLC), and a Phase 1 program in combination with the anthracycline doxorubicin, where we aim to deliver both cardioprotection and enhanced anticancer activity for solid tumour patients. For more information on Racura and our clinical programs see the recording of the Racura R&D Symposium https://vimeo.com/1185454105
About the Role
We are seeking an experienced physician to contribute to clinical development activities through investigator engagement, scientific collaboration, study execution support, and medical oversight. This role will report to the CEO and work closely with the Program Clinical Leads and other members of the Racura team to support investigator relationships, referral engagement strategies, and operational delivery across all of Racura’s clinical programs.
Key Responsibilities
- Support clinical development activities across Racura’s oncology programs, with a strong focus on investigator and medical community engagement
- Act as sponsor Medical Monitor across assigned clinical studies, supporting medical review, eligibility discussions, and safety oversight activities
- Build and maintain strong relationships with key opinion leaders (KOLs), investigators, referral networks and broader oncology networks
- Work with clinical program leads to develop and implement referral pathways and investigator engagement strategies supporting patient identification and study enrolment
- Lead and coordinate advisory boards, investigator meetings, and clinical engagement activities
- Serve as a key medical liaison to investigators and clinical sites during study start-up and conduct
- Provide medical support during site interactions, conferences, and external clinical meetings
- Contribute to protocol development, amendments, and other clinical documentation as required
- Partner cross-functionally with Clinical Operations, Regulatory Affairs, Scientific teams, Biostatistics, and program leadership to support study execution
- Maintain awareness of emerging oncology data, evolving clinical practice, and competitive developments relevant to Racura programs
Essential for the Role
- MD (or equivalent medical degree)
- Prior experience in drug development, clinical development, medical affairs, medical monitoring, or a related pharmaceutical/biotech role
- Strong interpersonal and communication skills, with confidence engaging academic and community healthcare stakeholders
- Ability to work autonomously while collaborating effectively within cross-functional teams
- Strong professional writing skills
Desirable for the Role
- Experience in oncology, including solid tumours and/or haematologic malignancies
- Experience building and maintaining relationships with KOLs, investigators, and referral networks
- Experience supporting advisory boards, investigator meetings, or scientific engagement activities
- Understanding of GCP, regulatory requirements, and clinical trial operations
- Experience in early-phase clinical development and/or investigator-sponsored studies
- Interest in working within a collaborative, agile, and entrepreneurial biopharma environment
Work Environment
Racura offers a flexible/work-from-home environment with regular face-to-face collaboration and periodic in-person company meetings. The role is suited to a self-starter who thrives in an agile biopharma environment and enjoys a collaborative, fast-paced culture that values intellectual curiosity, direct communication, and pragmatic problem-solving.
Travel Requirements
Willingness to travel up to 1 day a week on average, for activities including:
- Investigator and site engagement activities
- Advisory boards and investigator meetings
- Scientific conferences and company meetings
- Domestic and international travel as required
Remuneration Package
$345,000 – $400,000 package consisting of a base salary of $190,000 – $220,000 + 12% super + 20% cash performance bonus + 50% of base salary in equity (company options)
