Dr. Martinez-Torres has more than 25 years of professional experience and significant medical and pharmaceutical expertise in both academia and industry spanning basic, translational and clinical research in neuroscience, immunology and HIV. His pharmaceutical development expertise encompasses clinical programs spanning Phases I through IV, across diverse therapeutic platforms (e.g., small molecules, biologics, gene therapies) across numerous neurology areas, including rare disease with strong focus on acute brain injuries, neuro-infection and neuro-vascular diseases.

Dobrica Neric, MD, is a Medical Director for Oncology, based in Belgrade, Serbia. Dr. Neric is a specialist of Internal Medicine and sub-specialist of Medical Oncology and has more than 20 years of clinical experience as a physician. He has worked in several medical departments in primary, secondary and tertiary medical care institutions, including the General Hospital of Uzice to Institute for Oncology and Radiology of Serbia in Belgrade. His main focus are several areas within Medical Oncology with strong clinical background in all Internal Medicine departments (especially Cardiology). 

Dr. Neric graduated and completed further education of Internal Medicine specialization and Medical Oncology sub-specialization, on Medicine Faculty of University of Belgrade, Serbia. 

Dr. Neric started his CRO career as a Medical Officer and Medical Monitor and he has joined our company in February 2023. Currently, he is involved in Fortrea clinical trials as a Project Physician, for the Phases I, II and III of clinical trials and also cooperates with other Fortrea departments on different projects.

Diana Aguirre, MD, is Senior Medical Director in oncology for Fortrea Clinical Development Services, based in France. Dr. Aguirre has more than 25 years of experience in both oncology clinical practice and drug development within mid and large size Pharma companies, focused on solid tumors and systemic treatments development, planning and implementation of global oncology studies from phase II to phase IV and strategic interactions with different key stakeholders in oncology clinical development. 

Dr. Aguirre earned her Medical degree from the University of Caldas in Colombia and completed her Medical oncology training at the national Cancer Institute in Colombia. She completed a Masters degree in pharmacogenomics and molecular biomarkers in oncology at Paris XI University. She joined our company in January 2014.

Dr. Hoelscher is based in Austin, Texas with 24 years of CRO industry experience in a wide variety of therapeutic areas, most recently in the past 16 years focusing on medical monitoring in ophthalmology indications including: 

• Retinal: dry/wet AMD, Non-infectious Uveitis, DME, Macular edema in uveitis, Vitreomacular traction, Proliferative/non-proliferative diabetic retinopathy 
• Anterior indications: dry eye, Glaucoma/POAG 
• Gene therapy: wet AMD, Batten’s disease 
• Rare disease: Batten’s disease, choroideremia, Stargardt’s disease, Retinitis Pigmentosa, Leber’s amaurosis 

While in medical school, he participated in Parkland Hospital’s “Mavericks in Ophthalmology” program, leading to a long fascination with research and the clinical practice of vision care.

Darby Thomas, PhD, is the Scientific Director of Fortrea’s Rare Diseases, Advanced Therapies and Pediatrics Team (RAPT). She has more than 20 years of experience in virology, cell and molecular biology, gene and cell therapy and biotechnology. 

She also has broad experience in adeno-associated virus (AAV) gene therapy with roles in CMC, discovery, translational development and patient advocacy for several AAV-focused companies including AGTC, StrideBio, and Sio Gene Therapies with an emphasis on rare neurological diseases and ophthalmology. 

Before the formation of Fortrea, Dr. Thomas was the Director of the Labcorp Enterprise Cell and Gene Therapy team. She also worked as the Director of Rare Diseases at Intrexon, where she gained translational experience developing AAV and plasmid-based gene therapies as well as gene-modified cell therapies for the treatment of rare skin disorders.

Dr. Gandia is a physician with more than 30 years of experience in clinical oncology and the pharmaceutical industry. He is a former senior clinical permanent staff member of the Institute Gustave-Roussy (Paris, France) under the supervision of Professor Jean-Pierre Armand. He joined IQVIA on 2016 as Medical Director in the Therapeutic Science and Strategy Unit for the US, Canada and Latin-America regions and worldwide clinical trials in 2021, serving as Senior Medical Director. He joined Fortrea in February 2023 as Senior Medical Director, MedSci Therapeutic Expertise-Oncology & Global Clinical Development. 

He is Board Certified in Medical Oncology, with a special interest in Melanoma, Lung, Head and Neck, Colorectal and Breast Cancer. He has been continuously working in clinical and academic settings for more than 25 years. Dr. Gandia has also served as Scientific Advisor and Medical Director in several Pharmaceutical Companies during his professional career. 

Dr. Gandia received his Medical Degree at the School of Medicine of the University of Buenos Aires, Argentina, and he underwent his postgraduate training in Internal Medicine and Clinical Oncology at the Sanatorio Guemes, Buenos Aires, completing his Oncology fellowship program in 1988 and spending one extra year as Chief Resident and Instructor at the Instituto Angel H. Roffo (the Argentinean National University Cancer Institute). 

At the Institut Gustave-Roussy, he produced several publications in peer-reviewed journals and meetings abstracts in early phases of oncology drug development. 

He was heavily involved in the drug development of irinotecan. Dr. Gandia was the first investigator who described the drug cholinergic acute syndrome, and also as the head, one of the investigators that described the use of high-dose intense Loperamide to control delayed diarrhea during the European Phase I study. 

Dr. Gandia's top skills are oncology, Phase I-III studies, study design, biology and molecular oncology, pharmacology, publishing papers and providing educational programs for professionals. He joined our company in February 2023.

Dana Romano, MD, is a Senior Medical Director at Fortrea. In this position, she has the responsibility of leading the medical team working on global respiratory Phase I, II, III and IV studies, ensuring the Execution of the projects and direct communication with sponsors, including Medical Monitoring to support to Clinical Operations and Pharmacovigilance and ensure the development of compelling medical strategies and integrated solutions to meet sponsors’ needs. 

Dana started her pharmaceutical career as a Principal Investigator conducting Phase IV studies at her GP practice and Phase I and II studies at Richmond Pharmacology (Croydon University Hospital, UK), before moving to the Clinical Research Physician and Medical Monitor roles at Wyeth and Pfizer UK. 

Dana is board-certified in Family Medicine and has strong medical expertise gained through 11 years of clinical practice experience in Romania and the UK. She worked as a GP for 7 years at her own practice and with the largest private service providers. Dana has more than 21 years of experience in the pharmaceutical and CRO industry and managed successfully Phase I-IV clinical trials in biopharmaceutics, from the early protocol development through to medical oversight of enrolled adults, adolescents and children.

Claudia is Board Certified in nutrition and metabolism and offers 20+ years of pharmaceutical and CRO experience in Phase II-IV clinical research. Claudia joined Fortrea (previously Labcorp Drug Development) in 2014 and started building the Liver Therapeutic Area. She is currently heading the Liver medical team, responsible for the medical oversight and for providing strategic medical consultation. She is also chairing the Innovative Study Design working group. Claudia has comprehensive experience in leading drug development programs with her main focus in metabolics and liver indications. 

Claudia is a member of the Liver and PSC Forum, AASLD steatohepatitis working group and EASL NAFLD group. She has authored multiple manuscripts, including five recent review papers about clinical development in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) and adaptive design studies.

Chunyan Li, MD, is an associate medical director of oncology for Fortrea, based in China, Shanghai. Dr. Li has solid background and experience in Oncology, she is a board certified oncologist and has 7 years of clinical experience in Shanghai's top hospitals and has served as medical monitor in CROs since 2018 for studies that include solid tumors (non-small cell lung cancer, small cell lung cancer, hepatocellular carcinoma, gastrointestinal stromal tumor, colon cancer, head and neck squamous cell carcinoma) as well as lymphomas (classical Hodgkin’s lymphoma, mantle cell lymphoma, non-Hodgkin’s lymphoma). 

Dr. Li received her bachelor degree of clinical medicine from Shanghai Jiao Tong University School of Medicine and master degree in oncology from Tongji University and Shanghai Jiao Tong University School of Medicine. She completed the standardized training for residents and standardized training for oncology specialist in Fudan University Shanghai Cancer Center and Shanghai 10th People’s Hospital. She joined our company in May 2021.

Dr. Cheerag Shirodaria is the Vice President and Cardiovascular/Metabolic Therapeutic Area Head at Fortrea. He has over 25 years of clinical experience as an interventional and clinical cardiologist and remains on the Faculty at Oxford University Hospitals. He is an expert in cardiac imaging, having completed his doctoral thesis at the University of Oxford on the role of cardiovascular MRI in the evaluation of vascular function. He is also co-director of the coronary computed tomography angiography (CCTA) service in Oxford. He is also co-founder and Chief Development Officer of Caristo Diagnostics, an AI image analysis company that has developed proprietary AI image analysis technology that quantifies cardiometabolic risk associated with coronary inflammation plaque and adipose tissue characteristics. He has supported multiple companies through regulatory interactions, protocol development and Scientific Advisory Board interactions. 

Dr. Shirodaria received his medical degree from St. Bartholomew’s Hospital Medical College in London, his medical doctorate from the University of Oxford and his MBA from London Business School.