About Nutromics

At Nutromics, we exist to save lives through continuous diagnostic monitoring, and we want you on board!

Nutromics is developing a wearable diagnostic platform – the world’s first “lab-on-a-patch.” We're looking for people who are passionate about saving lives with ground-breaking, DNA-based, diagnostic technology.

We are growing quickly, expanding globally however, our passion for creating a better world will always be at the heart of it. Help us save millions of lives and change the face of healthcare.

About the Role

This is a leadership role that drives the strategic and operational aspects of Nutromics’ clinical studies for our cutting-edge wearable technology. You’ll be at the forefront of managing and leading clinical trial strategies, ensuring regulatory compliance, and providing clincial expertise in the diagnostic space.

Some of your responsibilities

• Lead the strategic design, initiation, and execution of clinical studies aligned with R&D strategies for FDA and TGA clearance.
• Provide strategic direction for clinical studies, including the design and implementation of clinical development programs (CDP) across medical device studies.
• Ensure clinical trials comply with regulatory standards (FDA, EMA, ICH-GCP), and lead protocol design and authoring.
• Collaborate with internal and external stakeholders including KOLs, clinical investigators, and business partners.
• Provide leadership ensuring the safety and well-being of study participants.
• Identify and manage risks associated with clinical trials, including participant safety, regulatory hurdles, and unforeseen delays.
• Oversee clinical trial budgets, track spending, optimize resources, and ensure on-time, on-budget trial execution.

Must have:

• 5-7 years of experience in the biotech or medical device industry, with at least 5 years managing clinical studies.
• Demonstrated in depth knowledge in GCP
• Expertise in regulatory requirements (FDA, EMA, ICH-GCP) and clinical study design.
• Hands-on experience authoring clinical study documents like protocols, Investigator Brochures, and Consent Forms.
• Familiarity with Human Research Ethics Committees, Data Safety Monitoring Boards, and site governance.
• Strong leadership skills and the ability to manage complex trial risks and compliance challenges.

Preferred:

• Diagnostics experience
• Medical Degree or AHPRA Registered Doctor

At Nutromics, we’re not just developing technology; we’re creating life-saving innovations. If you’re passionate about making a difference in healthcare, we want to hear from you.