Job Type: Permanent position | Full time position

Job Description

Medical Advisor Location: Melbourne, Australia The Medical Advisor delivers medical, clinical and scientific advisory expertise in clinical research studies and post marketing programs (RWI).

Signal detection and aggregated reporting. Essential Functions Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects

Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. May contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs).

May provide therapeutic area/indication training for the project clinical team. Attends and may present at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs).

May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. May perform medical review of adverse event coding.

Performs review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client meetings,



as needed or requested. Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.

Qualifications & Experience Medical degree (MD or equivalent) from an accredited and internationally recognized medical school. Specialist training and clinical experience as an Oncologist and/or Haematologist is preferred.

Current or prior medical license to practice medicine. Board certification or equivalent specialist recognition in oncology or hematology strongly preferred. Experience

Typically 3–5+ years of post graduate clinical experience; prior industry or clinical research experience highly desirable. Demonstrated experience in early phase oncology/hematology clinical trials (Phase I and/or first in human studies strongly preferred).

Experience in medical monitoring, protocol review, and safety oversight within a CRO, biopharmaceutical, or academic research setting is advantageous. Robust, current knowledge of: Oncology and/or hematology therapeutic landscapes

Clinical trial methodology and drug development Relevant global and local regulatory requirements (GCP, ICH, TGA, FDA, EMA) High level of scientific and clinical judgment, with a patient centric mindset.

Strong communication, presentation, and stakeholder engagement skills. Demonstrated business acumen and ability to contribute to strategic discussions .

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📌 Medical Advisor (Melbourne)
🏢 Iqvia Rds Pty.
📍 Melbourne