Medical Director

vor 13 Stunden

Council of the City of Sydney, Österreich Racura Oncology Vollzeit

Medical Director (Oncology) - Remote Join to apply for the Medical Director (Oncology) - Remote role at Racura Oncology. Overview ASX-listed oncology drug development company Full-time continuing position (remote) with competitive remuneration package Leadership of clinical development responsible for clinical medical and regulatory affairs Guidance and coaching from experienced leaders in oncology About The Company Racura Oncology (ASX:RAC) is an ASX-listed Phase 3 clinical biopharmaceutical company with a dedicated mission to be at the heart of cancer care. Racura’s lead asset, RCDS1 (E,E-bisantrene), is a small molecule anticancer agent that primarily functions via G‑quadruplex‑DNA & RNA binding, leading to potent inhibition of the important cancer growth regulator MYC. RCDS1 has demonstrated safe and efficacious activity in cancer patients. Racura is advancing a proprietary formulation of RCDS1, 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 1a/b program in mutant epidermal growth factor receptor non‑small cell lung cancer (EGFRm NSCLC), and a Phase 1a/b program in combination with the anthracycline doxorubicin, where we aim to deliver both cardioprotection and enhanced anticancer activity for solid tumour patients. About The Role We are seeking an outstanding physician for our growing number of clinical programs. Reporting to the Vice President of Medical, you will work closely with a number of internal and external cross‑functional teams to deliver Racura’s clinical programs in a timely and cost‑efficient manner. You are a self‑starter who is energetic and outgoing. You are focused on improving patients’ lives whilst building deep professional relationships with all external stakeholders. You deliver outstanding presentations and documents and can engage in peer‑level discussions with leading oncologists. You ideally will have experience working with regulators including TGA, FDA and EMA. You are agile and happy to be working in a fast‑paced environment where rapid change is the norm and where you can expect professional development from an industry leading team. Essential For The Role MBBS, MD or equivalent Minimum 8 years of experience working in clinical trials Proven track record of outstanding written and verbal communication Demonstrated cross‑functional collaboration Ability to build rapport and credibility with key clinicians, regulators, consultants, and other stakeholders A passion for oncology, clinical development, medical affairs and improving patient outcomes Attention to detail with the ability to think strategically and deliver operationally Ability to travel domestically and internationally as required by the company Desirable for the role MBA or other business qualification Experience in the development of oncology medicines Background in the pharmaceutical industry Knowledge and experience with regulatory and clinical practice in Europe, China and the US #J-18808-Ljbffr

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