TD2 Oncology

TD2 Oncology

TD2 Oncology is a full-service CRO specializing in complex cancer trials. We offer a comprehensive range of services across preclinical research, regulatory strategy, flow cytometry, and clinical trial management to help sponsors bring therapies to patients faster.

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Locations

  • APAC
  • Europe
  • North America

Therapeutic Areas

  • Oncology

We partner with biotech and pharmaceutical companies to advance novel cancer therapies through a comprehensive suite of services spanning preclinical research, regulatory strategy, clinical trial management, and specialty capabilities such as flow cytometry.

Founded in 2003 as a subsidiary of the Translational Genomics Research Institute (TGen), TD2 Oncology opened its doors on the Mayo Clinic campus in Scottsdale, Arizona. Our origins in translational science continue to shape our approach, blending deep oncology expertise with operational agility and scientific insight.

We support a wide range of therapeutic modalities and study types, including but not limited to radiopharmaceuticals, antibody-drug conjugates (ADCs), cell and gene therapies, and cancer vaccines. Our multidisciplinary team of scientists, clinicians, and regulatory experts is dedicated solely to oncology, bringing a deep understanding of cancer biology, trial complexity, and the evolving regulatory landscape. TD2 Oncology is expertly tailored to help sponsors navigate the unique challenges of cancer drug development. With focused expertise, personalized guidance, and a commitment to scientific excellence, we help sponsors overcome development hurdles and move their therapies forward with greater precision and speed.

Accreditations

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.
Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.
Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.