About Radiopharm Theranostics
Pioneering the Next Frontier in Radiopharmaceuticals
Our Mission
We are redefining oncology care with first-in-class radiopharmaceuticals - precise, targeted therapies that address significant gaps in care, enabling individuals with cancer to live longer, fuller lives.
Our Vision
A future where every cancer diagnosis has a targeted radiodiagnostic and radiotherapeutic solution—delivering hope to individuals with cancer beyond conventional therapies.
Purpose
Delivering innovative radiopharmaceuticals to transform cancer care globally.
What Sets Us Apart
Transforming precision cancer care by delivering innovative radiopharmaceutical solutions for the earlier detection and personalized treatment of cancers with unmet needs.
Science & Innovation
Clinical-Stage Momentum
Impact

Our Story
Founded in 2021 by biotech entrepreneur Paul Hopper, RAD emerged from a singular vision: to deliver innovative radiopharmaceutical solutions that have the potential to transform cancer care globally.
Today, as a dual-listed (NASDAQ: RADX / ASX: RAD) company with active clinical trials, we're translating that vision into a clinical reality.
Key Milestones Timeline
2021
ASX Listing
2022
MD Anderson Joint Venture Launched
2023
Initiated First-in-Human Trials
2024
NASDAQ Listing
2025
Initiated First PIIb Trial
Our Leadership
A global team with world-class radiopharmaceutical experience.

Paul Hopper, Founder
25+ years launching oncology innovators
"RAD isn’t just developing drugs—we’re rewriting oncology’s playbook."

























































Dr. Voliotis has 20 years of experience in the pharmaceutical and biotechnology sector in the US and Europe, with an emphasis on radiopharmaceuticals, and 12 years experience in academic preclinical and clinical research. He has held global drug development roles in large and medium sized pharmaceutical companies and start-up phase companies. He has designed and executed multiple registrational trials in numerous oncology indications, mutiple INDs (Investigational new drug applications), preclinical through to first in human trials and has overseen numerous regulatory submissions which have resulted in approvals for four drugs in eight different oncology indications. He was most recently Senior Vice President, Head of Clinical Development of radiopharmaceutical business Convergent Therapeutics. Prior to this he held the same role at oncology company Zentalis Pharmaceuticals (NASDAQ: ZNTL). He previously held a range of development roles with major German multinational pharma company Bayer AG as well as at Japanese company Eisai Inc. Dr Voliotis also recently acted as a Consultant in Oncology Drug Development with Magnesia Partners Consulting LLC, advising on clinical development and regulatory strategy.




Riccardo has broad and deep experience across specialty pharma, oncology and radiopharmaceuticals. He was most recently Chief Commercial Officer of Novartis company Advanced Accelerator Applications, one of the leading radiopharmaceutical and nuclear medicine companies globally. He was responsible for global commercial strategy and country organisations in ~20 countries across North America, Europe and Asia. He was lead for Lutathera in-market growth strategy and execution to build a blockbuster asset and lead on the prelaunch plan for Lu-PSMA 617 in metastatic prostate cancer. He assessed Go To Market Models for each priority country and access to other markets. Prior to this Riccardo was Senior Vice President and Global Head, Breast Cancer Franchise for Novartis Oncology since 2017, overseeing the launch of major breast cancer products including KISQALI and PIQRAY. He has also held various management roles with Novartis Pharma and Ethicon/Johnson&Johnson.




Paul is the Founder of Radiopharm Theranostics. He has over 25 years experience in the biotech, healthcare & life sciences sectors. Focussed on start-up and rapid growth companies, he has served as either Founder, Chairman, non-executive director, or CEO of more than fifteen companies in the US, Australia and Asia. Previous and current Boards include Imugene, Chimeric Therapeutics, Viralytics, Prescient Therapeutics, Polynoma. His experience covers extensive fund raising in US, Australia, Asia and Europe, and he has deep experience in corporate governance, risk and strategy. He also has many years experience in providing corporate advice and guidance, financial analysis and management of companies of differing sizes and financial circumstances.






Dr Mei-Ling Bermúdez joins Radiopharm Theranostics (RAD) as Manager of Analytical Development with over 15 years of interdisciplinary experience in spanning biotechnology, pharmaceuticals, CDMOs, and academic research. She has led analytical development, method validation, and instrumentation qualification across diverse biochemical and analytical techniques including HPLC/UPLC, LC/MS, GC/MS, PCR, nrCE/rCE, FTIR, UV/VIS, and immunoassays, ensuring compliance with cGMP, GLP, and global regulatory standards.
Dr. Bermúdez has managed cross-functional teams, developed, and transferred complex analytical methods for biologics and live biotherapeutics, and successfully supported pre-clinical through clinical drug development programs. Her scientific contributions include peer-reviewed publications, international presentations, and recognition through competitive awards and fellowships.
Dr. Bermúdez earned her Ph.D. in Environmental Genetics and Molecular Toxicology from the University of Cincinnati, an M.Sc. in Biochemistry and Nutrition, and a B.Sc. in Chemistry from the University of Puerto Rico. Fluent in English and Spanish, she brings a solution-driven mindset and a passion for advancing analytical innovation to support RAD’s mission in precision oncology care.




With more than 20 years of experience in clinical research, Jen has held a variety of roles across the industry. Based in Australia, she has worked with both small biotech companies and large pharmaceutical firms, as well as Contract Research Organizations (CROs) of all sizes. Jen has contributed to Phase 1 through Phase 3 studies across multiple therapeutic areas, including oncology, hematology, endocrinology, First in Human, rheumatology – among others. Most recently, Jen held the role of Project Director in the Early Phase group at George Clinical.



Core Responsibility
Our commitments in action:
Scientific excellence, regulatory compliance and the highest ethical standards to ensure that our differentiated radiopharmaceutical technologies improve clinical and patient outcomes, and contribute meaningfully to the early detection, diagnosis and treatment of cancers.
To the Oncology Community
Designing trials with real-world utilities to ensure our radiopharmaceuticals address unmet needs beyond trial endpoints.
To Global Partners
Through global strategic alliances, we secure isotope access and accelerate clinical and translational research.
To Stakeholder Trust
Every program prioritizes reproducible data and scientific rigor.
To Scientific Integrity
We pursue novel targets because individuals with cancer deserve truly differentiated therapies.
Join Us in Shaping the Future of Precision Oncology
Radiopharmaceuticals are rewriting cancer care—be part of the revolution.

