Medical Monitor (Gastroenterology) | Remote – Sydney, Melbourne

Date published: Sep 2, 2026, 10:40 AM

Location

Remote role, with Sydney or Melbourne preferred as your home location

Description

This is a senior medical role within a CRO's medical monitoring team.

You would provide medical oversight across clinical trials by:

  • protecting participant safety, assuring data integrity, and advising sponsors, sites and study teams on medical matters from protocol design through to final reporting
  • advising clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters
  • contributing to clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts and scientific presentations
  • reviewing and analysing clinical data to safeguard the safety of study participants
  • ensuring reported data is accurate, complete and verifiable, and that trial conduct complies with the approved protocol and amendments
  • addressing safety issues raised across the study by sites and the study team, and support pharmacovigilance activities
  • identifying program risks and implement mitigation strategies with Clinical Operations
  • organising and leading clinical development advisory boards and safety monitoring boards
  • participating in bid defence meetings
  • ensuring study-team compliance with local regulatory agencies, ICH and GCP guidelines
  • reviewing and signing off clinical documents for medical relevance

Essential qualifications

We're looking for someone with the following qualifications, experience and capabilities:

  • Medical Doctor (MD) degree
  • Board certification in Gastroenterology preferred
  • Prior experience in clinical research
  • Clinical experience in a major therapeutic area (oncology, infectious disease, gastroenterology, haematology or internal medicine) is desirable
  • Familiarity with clinical research practice and local regulations; experience of local health-authority interactions leading to drug approval is strongly preferred
  • Able to train clinical monitors and physician investigators, and build constructive, trusted relationships at all levels
  • Strong leadership, communication, presentation and organisational skills
  • Sound critical thinking and problem-solving, able to carry the role with minimal guidance
  • Proficiency with MS Office applications

Apply

To apply, contact:

Terry Cornick

Email terry@clinicaladvisors.com.au
Phone 0406 641 984

Applications close

Sep 30, 2026, 23:59 PM
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