A rare opportunity to become a key early hire in Australia for a well-funded, high-growth US life sciences company. This isn't a traditional Clinical Operations role where you inherit an established team and manage everything through a CRO. We're looking for someone who wants to get hands-on, take genuine sponsor-side ownership of Australian clinical studies, and help build the local clinical operation from the ground up.

• Own Australian clinical studies end-to-end from the sponsor side
• Lead HREC submissions, CTN/CTA pathways and Australian regulatory activities
• Work hands-on with protocols, study design, endpoints and trial delivery
• Collaborate directly with senior global scientific and clinical leadership
• Gain exposure to FDA strategy and globally aligned clinical development
• Work across decentralised trials, vendors, participants and study logistics
• Become a key early hire with the opportunity to build out the Australian team
• Meaningful equity participation alongside a strong base salary

• Strong Australian sponsor-side clinical trial experience
• Direct HREC and CTN/CTA experience
• Hands-on protocol development experience
• FDA / US regulatory exposure
• A strong scientific, medical or pharmaceutical background
• Experience operating in a smaller biotech, start-up or similarly hands-on environment

This will suit someone who wants more than simply managing studies. There is genuine scope to own the Australian clinical program, influence how studies are designed and delivered, and ultimately build a team around you as the business grows.

A rare opportunity to become a key early hire in Australia for a well-funded, high-growth US life sciences company. This isn't a traditional Clinical Operations role where you inherit an established team and manage everything through a CRO. We're looking for someone who wants to get hands-on, take genuine sponsor-side ownership of Australian clinical studies, and help build the local clinical operation from the ground up.

• Own Australian clinical studies end-to-end from the sponsor side
• Lead HREC submissions, CTN/CTA pathways and Australian regulatory activities
• Work hands-on with protocols, study design, endpoints and trial delivery
• Collaborate directly with senior global scientific and clinical leadership
• Gain exposure to FDA strategy and globally aligned clinical development
• Work across decentralised trials, vendors, participants and study logistics
• Become a key early hire with the opportunity to build out the Australian team
• Meaningful equity participation alongside a strong base salary

• Strong Australian sponsor-side clinical trial experience
• Direct HREC and CTN/CTA experience
• Hands-on protocol development experience
• FDA / US regulatory exposure
• A strong scientific, medical or pharmaceutical background
• Experience operating in a smaller biotech, start-up or similarly hands-on environment

This will suit someone who wants more than simply managing studies. There is genuine scope to own the Australian clinical program, influence how studies are designed and delivered, and ultimately build a team around you as the business grows.

Join a leading clinical research organisation as a Medical Officer supporting early-phase and healthy-volunteer studies. This role is ideal for doctors who enjoy fast-paced clinical work, structured protocols, and a strong focus on participant safety.

• Provide high-quality medical care to clinical trial participants, ensuring compliance with GCP standards and ethical guidelines.

• Act as Investigator on assigned studies, including consent discussions, eligibility assessments, and protocol-required procedures.

• Review medical histories, diagnostics, and adverse events to support safe trial conduct.

• Prescribe investigational and permitted concomitant medications within scope.

• Work closely with cross-functional teams across operations, pharmacy, QA, and project management.

• Participate in safety reviews, audits, on-call rotations, and continuous improvement initiatives.

• Medical degree and full, unconditional registration (minimum 2 years).

• Strong clinical judgement and recent hands-on experience.

• Advanced Life Support certification and current GCP training.

• Excellent communication skills and ability to engage with healthy volunteers.

• Comfortable working in a high-volume, time-sensitive clinical environment.

• Clinical trial experience is an advantage but not essential.

Planet Pharma in Brisbane is seeking a Medical Officer / Clinical Research Physician to support Phase I trials involving healthy volunteers and patients. You will provide medical oversight and supervise safety during early clinical development.

The role requires a medical degree with unrestricted AHPRA registration and strong clinical assessment skills, with experience in fast-paced trial environments and excellent stakeholder communication.