Emerald Clinical’s team will be attending PCT Congress 2025, November 17-18 in Boston.

Book a Meeting with our Team

Meet our Oncology Therapeutic Strategy Director, Vice President, Clinical Affairs, and Executive Director, Project Operations at PCT Summit 2025.

Oncology professionals will be gathering at Precision Clinical Trials Oncology Summit Boston 2025 to address challenges, explore revolutionary methodologies, and share success stories from ongoing and completed clinical trials. Meet with Emerald Clinical Trials’ experienced Oncology team who blends scientific integrity with operational intelligence to accelerate your oncology drug development program and help shape the future of cancer care.

Emerald Clinical has conducted over 440 oncology studies enrolling nearly 69,000 patients with 25% of those being Early Phase. Our long-standing relationships with global Oncology KOLs differentiate our collaborations. Their clinical experience combined with Emerald’s operational expertise ensure that your study addresses a real clinical need, is efficiently executed, respects patients, and will transition smoothly through phases and regulatory approvals.

Dr. Hegenberger is an MD, specialized in Internal Medicine, with an MBA, an MSc in Pharmaceutical Science, and postgraduate certifications from Georgetown University (International Business), Mount Sinai Hospital (Internal Medicine), and Harvard (Nanobiotechnology). He has 27 years of Pharma industry experience, including Country, Regional, and Global Medical Affairs and Clinical Research roles, having extensive experience in Clinical Operations, CROs’ supervision, Pharmacovigilance, Medical Information, and Safety.


Book a Meeting with our Team

The Emerald Clinical Oncology Advantage:

Our oncology team has over 20 years of cross-functional industry experience in all study aspects and expertise in:

  • Navigating rapidly shifting global regulatory environments
  • Strong feasibility studies for better site identification
  • Engaging Oncology KOLs for advice leading to faster recruitment and higher retention levels
  • Dedicated Early Phase teams and assistance with Australian R&D tax benefits
  • Access to qualified sites and patients in 70 countries
  • Creating early strategies that lead to faster regulatory approval and commercialization

Contact us to discuss our tailored solutions, and collaborative opportunities for your Oncology drug development program.

Meet our Team

Learn more about our Oncology Capabilities

Want to navigate the clinical trial environment with ease?

Book your meeting with our team today and learn more about how we can help you manage your oncology trials.