" \u003cdiv class=\"ja-job-details\"\u003e \u003ch2 class=\"title\"\u003eMedical Director, Oncology\u003c/h2\u003e \u003cdiv class=\"meta\"\u003e \u003cul class=\"classifications\"\u003e \u003cli data-id=\"23519\"\u003e Medical \u0026amp; Scientific \u003c/li\u003e \u003cli data-id=\"23520\"\u003e Medical Monitor \u003c/li\u003e \u003cli data-id=\"23521\"\u003e North America \u003c/li\u003e \u003cli data-id=\"23522\"\u003e Permanent / Full Time \u003c/li\u003e \u003c/ul\u003e \u003cp class=\"date-posted\"\u003e 23/10/2026 \u003c/p\u003e \u003c/div\u003e \u003cdiv class=\"description\"\u003e \u003cstrong\u003eBroad Purpose\u003c/strong\u003e\u003cbr\u003e Avance Clinical is a Contract Research Organisation which offers specialised services supporting drug development for the pharmaceutical and biotechnology industry.\u003cbr\u003e \u0026nbsp;\u003cbr\u003e The Medical Director, Oncology provides medical and scientific leadership across oncology clinical development programs and serves as a key subject matter expert within Avance Clinical\u0027s Oncology Centre of Excellence. The role is responsible for providing medical oversight, scientific guidance, protocol review and development support, safety expertise, and therapeutic leadership across all phases of oncology clinical research.\u003cbr\u003e \u0026nbsp;\u003cbr\u003e Working collaboratively with sponsors, investigators, Clinical Operations, Business Development, Biostatistics, Regulatory Affairs, Pharmacovigilance, and other cross-functional teams, the Medical Director supports the successful design, execution, and delivery of oncology clinical trials while ensuring scientific integrity, patient safety, data quality, and regulatory compliance.\u003cbr\u003e \u0026nbsp;\u003cbr\u003e The Medical Director also contributes oncology expertise to business development initiatives through sponsor engagements, proposal support, feasibility assessments, bid defense meetings, and strategic discussions, helping position Avance Clinical as a preferred partner for oncology drug development.\u003cbr\u003e \u0026nbsp;\u003cbr\u003e \u003cstrong\u003eCore Responsibilities \u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eProvide medical and scientific leadership for oncology clinical development programs, serving as Medical Monitor and oncology subject matter expert across study design, execution, and delivery.\u003c/li\u003e \u003cli\u003eReview subject eligibility, protocol compliance, safety events, and clinical data to support subject protection and data integrity.\u003c/li\u003e \u003cli\u003eProvide medical input into dose-escalation decisions, Data Review Committees, Safety Review Committees, and other study oversight activities.\u003c/li\u003e \u003cli\u003eSupport investigators by responding to protocol and medical inquiries and providing clinical guidance throughout study conduct.\u003c/li\u003e \u003cli\u003eDeliver oncology therapeutic area expertise across study teams and departments.\u003c/li\u003e \u003cli\u003eContribute to the design and review of clinical trial protocols, informed consent forms, study manuals, and other clinical documents.\u003c/li\u003e \u003cli\u003eAdvise on patient populations, inclusion/exclusion criteria, study endpoints, efficacy assessments, and safety monitoring requirements.\u003c/li\u003e \u003cli\u003eReview and interpret emerging clinical, scientific, and safety data relevant to assigned studies and therapeutic areas.\u003c/li\u003e \u003cli\u003ePartner with Regulatory Affairs, Medical Writing, Pharmacovigilance, and Clinical Operations teams to ensure high-quality study delivery.\u003c/li\u003e \u003cli\u003eParticipate in investigator meetings, sponsor meetings, safety discussions, and regulatory interactions as required.\u003c/li\u003e \u003cli\u003eProvide oncology training, mentoring, and scientific guidance to internal teams.\u003c/li\u003e \u003cli\u003eContribute medical expertise to business development activities including proposals, RFIs, RFPs, bid-defense meetings, and sponsor discussions.\u003c/li\u003e \u003cli\u003eSupport scientific presentations, publications, conference participation, and Oncology Centre of Excellence initiatives.\u003c/li\u003e \u003cli\u003eOther duties as directed by Line Management consistent with skills, experience, and qualifications.\u003c/li\u003e \u003c/ul\u003e \u0026nbsp;\u003cbr\u003e \u003cstrong\u003eDepartmental Responsibilities\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eAct as a key Oncology Centre of Excellence subject matter expert across all phases of clinical development.\u003c/li\u003e \u003cli\u003eProvide strategic oncology guidance to internal stakeholders and project teams.\u003c/li\u003e \u003cli\u003eSupport capability development initiatives within oncology and related therapeutic areas.\u003c/li\u003e \u003cli\u003eParticipate in departmental process improvements, training activities, and quality initiatives.\u003c/li\u003e \u003cli\u003eContribute to the maintenance and expansion of oncology knowledge resources, investigator networks, and key industry relationships.\u003c/li\u003e \u003cli\u003eCollaborate with cross-functional leaders to strengthen Avance Clinical\u0027s oncology service offerings.\u003c/li\u003e \u003cli\u003eRepresent Avance Clinical at scientific meetings, industry conferences, and sponsor engagements.\u003c/li\u003e \u003cli\u003ePromote a culture of scientific excellence, quality, compliance, and patient safety.\u003c/li\u003e \u003c/ul\u003e \u0026nbsp;\u003cbr\u003e \u003cstrong\u003eQualifications, Skills and Experience\u003c/strong\u003e\u003cbr\u003e \u003cul\u003e \u003cli\u003eMedical degree (MD or equivalent) required.\u003c/li\u003e \u003cli\u003eSpecialist training, board certification, fellowship, or equivalent qualification in Oncology, Hematology-Oncology, or a related oncology discipline preferred.\u003c/li\u003e \u003cli\u003eSignificant experience in oncology clinical research, preferably within CRO, biotechnology, pharmaceutical, academic research, or healthcare environments.\u003c/li\u003e \u003cli\u003eDemonstrated experience serving as a Medical Monitor or providing direct medical oversight for oncology clinical trials.\u003c/li\u003e \u003cli\u003eStrong understanding of oncology drug development, clinical trial methodology, safety monitoring, and regulatory requirements.\u003c/li\u003e \u003cli\u003eExperience supporting early-phase and/or mid-phase oncology studies, including dose-escalation and complex clinical development programs.\u003c/li\u003e \u003cli\u003eSound clinical judgment with the ability to assess patient safety, protocol compliance, and emerging clinical data.\u003c/li\u003e \u003cli\u003eAbility to communicate complex medical and scientific concepts effectively to sponsors, investigators, and internal stakeholders.\u003c/li\u003e \u003cli\u003eExperience collaborating effectively within multidisciplinary clinical research teams.\u003c/li\u003e \u003cli\u003eExcellent written and verbal communication skills.\u003c/li\u003e \u003cli\u003eAbility to mentor and provide scientific leadership within a matrix environment.\u003c/li\u003e \u003cli\u003eExperience contributing to proposals, sponsor interactions, and business development activities preferred.\u003c/li\u003e \u003cli\u003eEstablished professional relationships within the oncology community are advantageous.\u003c/li\u003e \u003cli\u003eWillingness and ability to travel as required for sponsor meetings, conferences, and business needs.\u003c/li\u003e \u003c/ul\u003e \u0026nbsp; What You\u0027ll Receive\u003cbr\u003e \u003cul\u003e \u003cli\u003eCompetitive salary package\u003c/li\u003e \u003cli\u003eFlexible work arrangements\u003c/li\u003e \u003cli\u003eIndustry-leading technology and systems\u003c/li\u003e \u003cli\u003eDiverse, intellectually stimulating projects\u003c/li\u003e \u003cli\u003eClear career progression opportunities\u003c/li\u003e \u003cli\u003eSupportive leadership team and collaborative culture\u003c/li\u003e \u003cli\u003eLong-term stability with a growing global CRO\u003c/li\u003e \u003c/ul\u003e \u003cstrong\u003eAbout Avance Clinical\u003c/strong\u003e\u003cbr\u003e Avance Clinical is a leading Australian CRO providing specialised drug development services to the biotechnology and pharmaceutical industries. With origins dating back to the 1980s, we have built an outstanding reputation for quality, service excellence and innovation. Today, we partner with biotech companies globally to accelerate the development of new medicines.\u003cbr\u003e \u0026nbsp;\u003cbr\u003e \u0026nbsp;\u003cbr\u003e \u0026nbsp;\u003cbr\u003e \u0026nbsp; \u003c/div\u003e \u003cdiv class=\"apply\"\u003e \u003ca class=\"back-link\" href=\"#\" title=\"Back to search results\"\u003eBack to search results\u003c/a\u003e \u003cinput type=\"button\" class=\"ja-button\" data-job-id=\"919540\" value=\"Apply Now\" title=\"Apply Now\" /\u003e \u003c/div\u003e \u003c/div\u003e "