Oncology Publications 

Kamal Saini, MD, executive medical director at Fortrea Inc., is a board-certified medical oncologist based in Cambridge, United Kingdom, where he also practices part-time at the Addenbrooke’s (Cambridge University) Hospital. He contributes to the scientific strategic leadership of the oncology therapeutic area at Fortrea and provides clinical and medical expertise to project teams and other Fortrea departments on clients’ drug development projects. He liaises with key opinion leaders and academic cooperative groups with regard to the design, setup, and execution of cancer trials, especially in the breast cancer subdomain. He manages a team of high-performing medical monitors who are a part of the European oncology team. He leads the Precision Medicine and Emerging Therapies Leadership Center at Fortrea, and is also our global Scientific Publications Lead (Oncology). He brings more than 15 years of experience in clinical research and development to Fortrea. He is the author or co-author of several peer-reviewed journal articles. He joined our company in 2015.

Publications

• The Evolving Landscape in Multiple Myeloma: From Risk Stratification to T Cell-Directed Advanced Therapies
• Unraveling the link between cholesterol and immune system in cancer: From biological mechanistic insights to clinical evidence. A narrative review
• CAMBRIA-1 & CAMBRIA-2 phase III trials: camizestrant versus standard endocrine therapy in ER+/HER2– early breast cancer
• Bladder Cancer, Loss of Y Chromosome, and New Opportunities for Immunotherapy
• The Convergence of Radiology and Genomics: Advancing Breast Cancer Diagnosis with Radiogenomics

Luca Cantini, MD, PhD, is Medical Director at Fortrea, based in Leiden, the Netherlands. Dr. Cantini has 8 years of experience in oncology clinical drug development from academia to CROs, dealing with all aspects of early and late phase clinical trials. As a Medical Oncologist, he has been actively involved in translational research in Immuno-Oncology with a special focus on thoracic cancers. He earned his medical degree from the University of Pisa, Italy and completed his medical oncology fellowship training at the Polytechnic University of Marche, Ancona, Italy. In 2020, he was awarded with the ESMO Translational Research Fellowship, to carry on a project titled “ENSURE study - dENdritic cell therapy combined with SURgEry in mesothelioma” at the Erasmus MC, Rotterdam, the Netherlands. During the Fellowship, he decided to pursue a PhD trajectory at the same Institution, which has been finalized in 2022. Besides the ESMO Fellowship, he has been awarded with the IASLC Early Career Education Award, the ESO Grant for participating to the “18th ESO/ESMO Masterclass in Clinical Oncology,” the ESMO Grant for participating to the “Translational Research Unit Visit,” the ESMO Travel Grant for participating to the “2022 European Lung Cancer Conference,” and the NRS Travel Grant. He has authored 53 manuscripts in peer-reviewed journals. He joined our company in December 2022.

Publications

• Determinants of 5-year survival in patients with advanced NSCLC with PD-L1≥50% treated with first-line pembrolizumab outside of clinical trials: results from the Pembro-real 5Y global registry
• Unraveling the link between cholesterol and immune system in cancer: From biological mechanistic insights to clinical evidence. A narrative review
• Differential impact of lipid profile according to neutrophil-to-lymphocyte ratio status in patients with advanced cancer treated with immunotherapy
• Biomarkers in head and neck squamous cell carcinoma: unraveling the path to precision immunotherapy
• Neoadjuvant therapy in hormone Receptor-Positive/HER2-Negative breast cancer

Maria Ignacia Berraondo, MD, is Executive Medical Director and Head of Americas Oncology Therapeutic Expertise. Is a board-certified medical hematologist based in Buenos Aires, Argentina. Dr. Berraondo has +12 years of experience in clinical research, providing clinical and medical expertise to project teams and other Fortrea departments to advance clients’ drug development programs and contributing to the planning and execution of the scientific strategic leadership of the Oncology-Hematologic therapeutic area.

She manages a team of high-performing medical monitors who are part of the North America and Latin America oncology team. She leads the Hematologic Leadership Center at Fortrea, and contributes to strategic partnership development in the region.

Publications

• Equitable inclusion of diverse populations in oncology clinical trials: deterrents and drivers
• Antibody-drug conjugates, immune-checkpoint inhibitors, and their combination in advanced non-small cell lung cancer

Ken has over 30 years Clinical development experience across CROs, pharma & Biotech. He has significant experience from Pre-clinical validation, Global Clinical development planning, Program study execution and reporting, including licence application and approval to post registrational medical affairs activities.

With significant experience leading project management groups globally for over 20 years, through his 8 year tenure at FORTREA he transitioned from leading the PM group into a leadership role integrating the end to end solutions for Labcorp from preclinical through clinical & Laboratory services. In his current role he globally leads the Strategic Delivery and Growth team for Oncology, who are tasked with establishing compelling strategies aligned with our customers clinical development needs from FTIH Phase I to pre and post registrational study planning and delivery.

The primary focus for his team is leveraging the internal and external resources available to ensure a robust data driven study delivery strategy is established for clients needs and then working closely with the operational team to ensure delivery of that strategy. Although aligned to Oncology this team is truly cross therapeutic in background and experience from Cell and Gene therapy, immune-Oncology, radiotherapeutics, auto-immune disease and beyond to devices.

• 26+ years of drug development experience specializing in immuno-oncology in Pharma/Biotech and CRO environments
• Provides operational executive leadership for Oncology study portfolio at Fortrea
• Chief Development Officer experience managing cancer vaccine clinical development program
• Pragmatic and innovative Clinical Development Leader, building and managing early phase immuno-oncology portfolios, and operationalising various early/late phase protocols and programs in Oncology and Cell & Gene Therapy field

Laura Vidal, MD, is a certified medical oncologist with extensively experience in oncology drug. She holds two fellowships in Clinical Drug Development from the Royal Marsden hospital, London and the Princess Margaret Hospital, Toronto. She spent 15 years in clinical and academic positions specializing in the field on oncology and drug development. Throughout her career, Dr. Vidal has authored or co-authored dozens of peer-reviewed journal articles and received numerous health and research awards. Her research interests are focused on early phase development of targeted agents, molecular and imaging biomarkers and anticancer immunotherapy. She holds a thesis title from the London University in oncolytic viruses from her pre-clinical and clinical work in reovirus (Reolysin®). 

She joined our company in December 2020. Dr. Laura Vidal is the Medical Head of the Oncology group in EU. She contributes to the development of Fortrea policies involving medical, safety and therapeutics; serves as point of contact for key clients on business and studies oversight; manages relationships with investigators/sites for clinical trials, and mentors clinical research physicians and medical directors across the company.

Publications

• The Evolving Landscape in Multiple Myeloma: From Risk Stratification to T Cell-Directed Advanced Therapies
• Bladder Cancer, Loss of Y Chromosome, and New Opportunities for Immunotherapy
• Equitable inclusion of diverse populations in oncology clinical trials: deterrents and drivers
• Cancer Trials Ecosystem in India—Ready for Prime Time?
• Biomarkers in head and neck squamous cell carcinoma: unraveling the path to precision immunotherapy

Kazuya Iwamoto, MD, PhD, MBA, FACP, is Senior Medical Director for Fortrea in Osaka, Japan. He provides medical and scientific expertise to oncology study teams on clients’ drug development projects and contributes to the development of medical strategies and execution of clinical trials. Dr. Iwamoto has more than 25 years of experience as a physician, research clinician and medical director. 

Before joining Fortrea, he was Head of the Medical Division, including Clinical Development and Medical Affairs, for Hospira Japan in Osaka. He previously served as Head of the Medical Division for Biogen Idec, Head of Medical Affairs for Bayer Yakuhin, and Clinical Research Physician for Eli Lilly in Japan. Currently President and Fellow of the Japanese Association of Pharmaceutical Medicine, Dr. Iwamoto joined our company in May 2016.

Publications

• Biomarkers in head and neck squamous cell carcinoma: unraveling the path to precision immunotherapy

Krane Huang, MD, is a Senior Medical Director, China Regional Head of Oncology for Fortrea, based in Shanghai, China. Dr. Krane has nearly 20 years of experience as medical oncologist in cancer hospitals, global pharmaceutical industries and CROs, focused on planning and execution of global oncology clinical development projects in all phases (I-III), different drug types and classes. 

Dr. Krane earned his medical degree from Tongji Medical College, Huazhong University of Science & Technology and completed his internal medicine degree and medical oncology fellowship training at Wu Union Hospital. He joined our company in September 2019.

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.

Victor Angélico, MD, is a Senior Medical Director for Fortrea, based in Paris, France. He provides clinical and medical expertise to project teams and other Fortrea departments to advance clients’ drug development programs. Dr. Angélico performs medical monitoring on assigned projects; reviews protocols, case report forms and other data and materials, and contributes to the scientific leadership of the Oncology area at Fortrea with a special focus in early phase clinical studies and hematological malignancies. 

Dr. Angélico is board-certified in Internal Medicine and Oncology with 16 years in the clinic and has significant medical and pharmaceutical expertise with 14 years of experience in the pharmaceutical industry. Before his current position, he served as Senior Medical Officer for Chiltern, France and as Medical Director at IQVIA France. Dr. Angelico joined our company in January 2019.

Liliana Baila, MD, is Senior Medical Director for Fortrea, based in Brussels, Belgium. She serves as lead project physician on clients’ drug development projects. Dr. Baila provides medical/scientific support to project teams, performs medical and safety monitoring on assigned projects, and develops and reviews protocols, case report forms and other data and materials. Dr. Baila has more than 25 years of experience as a physician, research clinician and medical director. Before joining Fortrea, she served as Clinical Research Physician for the European Organization for Research and Treatment of Cancer (EORTC) in Brussels. Dr. Baila began her career as a physician training in neonatology and pediatrics at University Hospital in Romania. She joined our company in June 2020.

Moez Benali, MD, PhD, Senior Medical Director at Fortrea, also member of our global medical team, holds a medical degree and board certification in oncology supported by a PhD in molecular biology and anti-cancer drug development. He has over 22 years of overall working experience, 17 of which have been within the pharmaceutical industry (J&J, GSK, BMS, SOBI and Novartis Oncology) across Europe. As a well-rounded medical affairs and clinical development strategist, he has led activities across the life cycle drug development, and registered and launched 11 drugs at EMA, nine of them being the standard of care. 

Dr. Benali is a member of several cooperative groups such as ELN, EORTC and EBMT and head of Oncologues Sans Frontières. He joined our company in October 2022.

Publications

• CAR-T-Cell Therapy in Multiple Myeloma: B-Cell Maturation Antigen (BCMA) and Beyond

Carmen Besliu, MD, is Senior Medical Director in Bucharest, Romania. She serves as global lead project physician on clients’ drug development projects and provides medical/scientific expertise to project teams. Dr. Besliu reviews medical data and other materials, is responsible for medical and safety monitoring, and provides training in disease states and protocol-specific requirements to advance knowledge of good clinical practices across the company. She has more than 25 years of experience as a physician, research clinician, medical affairs head, and medical director. Before joining Fortrea, she was Oncology Medical Affairs Head for Novartis Pharma Services in Bucharest. She also has held medical affairs and clinical research positions with Baxter Healthcare, Sandoz, Roche, and AstraZeneca. Carmen joined our company in February 2021.

Publications

• The Evolving Landscape in Multiple Myeloma: From Risk Stratification to T Cell-Directed Advanced Therapies

Olga Bodriagova, MD, PhD, is a Medical Director in Oncology for Fortrea Clinical Development Services, based in Kyiv, Ukraine. Dr. Bodriagova has more than 20 years of experience in oncology clinical drug development as an Investigator, CRA and Medical Monitor in all phases of clinical development projects from early phase to post approval in different therapeutic areas, mainly oncology and women’s health. Dr. Bodriagova is serving as global lead project physician, providing medical and safety monitoring on assigned projects. 

Dr. Bodriagova earned her medical degree from the Kyiv Medical Institute in Ukraine and completed OB/GYN residency at the Kyiv City Hospital #2. Dr. Bodriagova received an oncogynecology certification from the Kyiv Institute of Postgraduate and defended her PhD thesis in the field of endocrine gynecology. She joined our company in 2014.

Publications

• Bladder Cancer, Loss of Y Chromosome, and New Opportunities for Immunotherapy
• Recent Advances in Gynecological Malignancies: Focus on ASCO 2023

Patrícia Andrade Brandalise, MD, is a boarded clinical oncologist in Brazil since 2005. Dr. Brandalise earned her MD and MsC degrees at Campinas State University (UNICAMP), Brazil, and received her oncology qualifications in the Campinas Institute of Oncology. She is an active member of the Brazilian Society of Oncology. 

Dr. Brandalise has more than 18 years of experience in clinical oncology with clinical, investigational and administrative responsibilities and 15 years serving in pharmaceutical industry. Prior to joining Fortrea, Patrícia worked for Janssen and Abbvie as Medical Director for Latin America in the Hematology and Oncology Business Unit. She also served as Oncology Medical Leader for Roche Brazil implementing several compassionate use programs in Latin America, preparing and delivering launches for new molecules/indications. She also has been designing and implementing Phase I-II-III-IV trials in Argentina, Brazil, Colombia, México, Peru, Argentina, Puerto Rico, Korea and Australia, many as lead physician.

Oxana Bzhadug, MD, PhD, is a Medical Monitor of Fortrea's global team, based in Moscow, Russia. Dr. Bzhadug has significant medical and pharmaceutical expertise with 14 years in the industry. Dr. Bzhadug received extensive scientific and clinical experience as a medical oncologist at Cancer Research Center (Moscow, Russia) for nine years. She has more than 23 years of experience in clinical trials, starting as sub-investigator in Phase I-III clinical trials and continuing in the industry supporting Phase I-IV trials within biotech (Amgen) and CRO. 

Dr. Bzhadug earned her Medical Degree in Moscow Medical and Dentist University and completed her Medical Oncology Fellowship in Cancer Research Center (Moscow). She has PhD degree in molecular biology of Breast Cancer. She joined our company in 2019.

Dr. Paulina Czajka-Francuz is a clinical oncologist with more than 25 years of experience in clinical trials. Acute hematological malignancies, as well as mechanisms of cancer resistance, have always been her main scientific interests. At Fortrea, Dr. Czajka-Francuz is primarily involved in Phase I and II hematological and oncological clinical trials.

Ashok Deenabandu MD is a Medical Director for Oncology at Fortrea, based in India supporting Asia-Pacific and EU region. With over 20 years of experience-including 14 years in global clinical development-Ashok has led numerous drug and device trials across leading CROs and product companies. He has served as Medical Lead for multiple global studies for both large pharmaceutical sponsors and emerging biotech firms.

His domain expertise includes both Immuno oncology and Cell/gene therapies, with focussed interest in lung cancer,hepatocellular carcinoma,gastric cancer,sarcoma,radiopharmaceuticals-in neuroendocrine,prostate cancers and early-phase trials involving CAR-T and CAR-NK cell therapies targeting solid tumors.

As a core member of the Global Oncology Team at Fortrea, he focuses on advancing clinical operations in India and the Asia-Pacific region. His role integrates scientific leadership with strategic oversight, supporting regulatory compliant trial design, cross-functional process optimization, and engagement with investigators and key opinion leaders (KOLs) to ensure successful study delivery.Throughout his career, he has demonstrated a consistent ability to translate regulatory insights into actionable business strategy, supporting global submission efforts, and shape internal frameworks that enhance operational excellence and client engagement.

Ashok is board certified Physician with specialist training in Radiology and Clinical Oncology from TN Dr MGR Medical University,India.He has also completed Fellowship in Epidemiology and Biostatistics from the University of New South Wales, and holds an advanced training credential in Cell and Gene Therapy from Yong Loo Lin School of Medicine/ACTRIS, Singapore, thereby broadening his expertise in translational research and cutting-edge therapeutic modalities.

Marco Durini, MD, PhD, is senior medical director of oncology for Fortrea, based in Milano, Italy. He brings more than 25 years of experience in clinical research for CRO and Pharma. Before joining the company, he held medic positions with Ipsen, Pfizer, Sanofi, Roche. His expertise in oncology ranges from biomarkers/precision medicine to immuno-target therapies and vaccines in solid and non-solid malignancies. Oncogenomics and Radiomics are latest areas of interest. 

Dr. Durini is board certified medical doctor at the Milan physician registry, and hold a business school training mastership at the SDA Bocconi Milan. He received his medical degree with summa laude from the University of Milan in Italy, and a granted post-degree research fellowship at ICP - University of Milan. He is author of papers submitted to ESMO/ASCO congresses. He joined Fortrea (formerly Labcorp) early 2019.

Carolina Dutra, MD, is a Medical Director for Fortrea Clinical Development Services, based in Brazil. She is medical oncologist by training and provides clinical and medical expertise to project teams and other Fortrea departments to advance clients’ drug development programs. Dr. Dutra performs medical and safety monitoring on assigned projects, develops and reviews protocols, case report forms and other data and materials, and contributes to the scientific strategic leadership of the oncology area at Fortrea. Dr. Dutra has more than 15 years of experience as a physician and principal investigator. She joined our company in May 2021.

José Espinoza, MD, is a Senior Medical Director, Therapeutic Area/Oncology at Fortrea, based in Madrid, Spain. Dr. Espinoza has over 20 years of experience in drug development, which includes enrolling patients into cancer trials, helping design and executing studies, medical monitoring and data analysis of global trials, interfacing with regulatory bodies, and working with biotech and pharmaceutical companies to refine drug development strategies. 

As a European board-certified onco-hematologist, Dr. Espinoza holds a double specialization: Clinical Oncology (1992-97) and Clinical Hematology & Bone Marrow Transplantation (1997-2001), and has more than 20 years of clinical experience as Consultant Onco-Hematologist at public hospitals in Spain and Ireland. Dr. Espinoza joined in our company in October 2021.

Publications

• The Evolving Landscape in Multiple Myeloma: From Risk Stratification to T Cell-Directed Advanced Therapies

Jose Daniel Fanjul Fuente, MD, is a Medical Director, Oncology, for Fortrea, based in Madrid, Spain. He provides medical and scientific guidance and support to project teams and investigative sites on clients’ drug development projects, and reviews protocols, case report forms, clinical study reports and other data and materials. Dr. Fuente has more than 10 years of experience as a physician and medical director in clinical research and development specializing in oncology. 

Before his current position, he held medical director and manager positions in oncology with IQVIA and Bristol Myers Squibb in Buenos Aires, Argentina. At Bristol Myers Squibb, Dr. Fuente led scientific activities that gave impetus to the product line of the oncology therapeutic area (Nivolumab and Ipilimumab). He joined our company in October 2018.

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.

Maria Paula Ghirardi, MD, is Medical Director of Oncology for Fortrea Clinical Development Services, based in Buenos Aires, Argentina. Dr. Ghirardi has 6 years of Oncology clinical research experience in both pharmaceutical and CRO industry. She provides clinical and medical expertise to project team and other Fortrea departments to advance clients’ drug development programs and contributes to the scientific strategic leadership of the Oncology therapeutic area. She has experience leading important launches of hematology-oncology compounds for multiple myeloma, AL amyloidosis, non-Hodgkin’s lymphoma, and chronic lymphocytic leukemia. 

Dr. Ghirardi earned her medical degree from the University of Buenos Aires and completed her internal medicine residency at the Hospital Ramos Mejia in Buenos Aires and Hematology residency at the Hospital de Clinicas in Buenos Aires and Sociedad Argentina de Hematologia. She joined our company in October 2022.

Brian Hamilton, MD, PhD, is Senior Medical Director for Fortrea, based in Newton, Massachusetts. He serves as Fortrea Subject Matter Expert for cellular immune-oncology, CAR-T and gene therapy. He also serves as global lead project physician on clients’ drug development projects. Dr. Hamilton has more than 35 years of experience in pediatric medicine, immunology, hematopoietic stem cell transplantation, and clinical research and development. Before joining Fortrea, he served as Executive Medical Monitor for Chiltern International. He has also held senior-level medical director, director physician, regulatory affairs and clinical research positions with Galena Biopharma, AstraZeneca, Onyx Pharmaceuticals, Wyeth Oncology, and other pharmaceutical and biotech firms. Dr. Hamilton joined our company in August 2018.

Konstantin Haradinov, MD, is a Medical Director, Oncology for Fortrea, based in Sofia, Bulgaria. He contributes to the development of Fortrea policies involving medical, safety and therapeutics; serves as global lead project physician and provides medical and safety monitoring on assigned projects; reviews medical data and provides clinical and medical expertise to project teams and other Fortrea departments, and performs safety trend analyses. 

Dr. Haradinov has more than 15 years of experience in clinical research as a medical director and physician/oncologist. Before joining Fortrea he served as Medical Officer, Oncology, for Chiltern International in Sofia, Bulgaria. Dr. Haradinov joined our company in April 2019.

Jinju Kim, MD, PhD, is a Medical Director of Oncology for Fortrea, based in Seoul, Korea. Dr. Kim has over 10 years of clinical development/clinical research experience in pharmaceutical industry and academia including a broad range of clinical drug development activities and cross functional collaboration. 

Dr. Kim earned her medical degree from Hanyang University and majored in Internal Medicine at Hanyang University Graduate School, Korea. In addition, she completed her internal medicine residency and fellowship training at Hanyang University Hospital and then worked as clinical physician and research professor. She has worked for various clinical and project-facing roles as a medical lead at both global pharmaceutical and innovative biotech companies since 2015. She joined our company in 2022.

Marcin Koziej, MD, is a medical director of oncology for Fortrea based in Warsaw, Poland. Dr. Koziej has more than 33 years of experience in medical onco-pulmonary research centers, CROs and the pharmaceutical environment. His roles have included physician and investigator, clinical operations professional and project management leader of pan-European and global teams, medical monitor and advisor, clinical strategist, business advisor and mentor. 

Dr. Koziej earned his medical degree from the Warsaw Medical School, Warsaw, Poland and completed his internal medicine fellowship at the National Research Institute for Tb and Lung Disease in Warsaw, Poland. In 2016 he joined Chiltern, which then became part of Labcorp in 2020 and is now Fortrea.

Publications

• Neoadjuvant therapy in hormone Receptor-Positive/HER2-Negative breast cancer
• Intracellular DNA sensing by neutrophils and amplification of the innate immune response

Carlo Lanza, MD, PhD, is Executive Medical Officer for Fortrea, based in Lugano, Switzerland. Dr. Lanza performs medical monitoring and safety assessments on Phase I-IV clinical trials for Fortrea clients. He leads early phase and translational research early development programs with targeted therapies, small molecules, biologics and gene therapy. Dr. Lanza also oversees development of late-stage development strategies, delivery and approval of registrational programs. He brings more than 20 years of experience in clinical research and development as a physician and medical director, specializing in pediatrics and oncology. 

Before joining Fortrea, he served as Medical Director for Medicines for Malaria Venture in Geneva, Switzerland. Dr. Lanza has also held leadership positions with Novartis Oncology, Pfizer Global R&D, and AstraZeneca UK. Carlo joined our company in 2012.

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.

Board-certified medical oncologist and nuclear medicine physician with over 20 years of hands-on experience in medical oncology and nuclear medicine and 15 years in the pharma industry. Her expertise spans various domains, including clinical development, regulatory affairs, safety, and medical affairs. Orchestrated successful product launches across diverse therapeutic areas including immunotherapies, targeted therapies, and cellular therapies. 

As a medical affairs expert, she has collaborated with healthcare professionals, patients, and payers to optimize treatment outcomes. Her deep understanding of trial design, patient recruitment, and data analysis has been instrumental in bringing novel treatments to patients.

Paulo Nunes, MD, is an Oncology Medical Director based in Porto Alegre, Brazil. Dr. Nunes is a medical oncologist and epidemiologist with more than 10 years of experience in oncology clinical and epidemiological research both as an investigator and medical monitor and has worked both in the academic setting as well as in cooperative oncology groups. His main areas of scientific interest are early-phase clinical trials, epidemiological studies, and gynecological cancers. 

Dr. Nunes earned his medical degree from the Federal University of Rio Grande and completed his internal medicine residency at the Hospital de Clínicas de Porto Alegre, medical oncology residency at Hospital São Lucas da PUCRS, and a fellowship in gynecological cancer and phase I clinical research at McGill University, Montreal, Canada. He holds a master's degree in Epidemiology from the Federal University of Rio Grande do Sul. He joined our company in March 2022.

Publications

• Immune Checkpoint Inhibitors in Breast Cancer: A Narrative Review

Maksym Novikov, MD, is a Senior Medical Director for Fortrea, based in Maidenhead, United Kingdom. He serves as global lead project physician on assigned projects, providing medical expertise and support in the development and conduct of clinical trials. This includes reviewing feasibility of investigator sites and recruitment of trial subjects and performing feasibility risk assessment and data safety monitoring, develops and reviews protocols, case report forms and other data and materials on assigned projects. 

Dr. Novikov has more than 20 years of experience as a physician (surgeon), clinical researcher and medical director. Before Fortrea, he was Senior Medical Officer for Chiltern International in the UK. He also has held clinical research and medical monitoring positions with Novartis, AstraZeneca and other drug development and health care organizations. He joined Fortrea in April 2019.

Zehra Nurgul Pamuklar, MD, PhD, is a Senior Medical Director of Oncology for Fortrea, based in Cary, North Carolina. Dr. Pamuklar has more than 20 years of experience in oncology clinical drug development in biotechnology companies and CROs. She has supported planning and execution of global oncology clinical development projects from early phase to post approval, within medical affairs and clinical development organizations, and management of pharmaceutical, academic and regulatory interactions. 

Dr. Pamuklar graduated in medicine from the Ankara University School of Medicine, Ankara, Turkey; she has a PhD in Physiology/Immunophysiology and a Master of Science Degree in Clinical Research Management from Duke University, Durham, NC. 

Before joining our company in 2019, Dr. Pamuklar provided medical management of Phase I to Phase III immuno-oncology/oncology clinical trials in non-small cell lung cancer, hepatocellular carcinoma, bladder cancer, esophageal carcinoma, melanoma, pancreatic cancer, prostate cancer, urothelial cancer, colorectal cancer and head and neck cancer.

Lingjuan Pang, MD, is a Medical Director of oncology for Fortrea Clinical Development Service, based in Guangzhou, Guang Dong Province, China. Dr. Pang as a member of our global team of Medical Monitors has significant medical and pharmaceutical expertise with 14 years in the industry. She has vast knowledge of oncology therapeutic experience across Phase I-III. She has built strong relationships with external research groups and Key Opinion Leaders (KOLs) to which our experience and success ensures optimal performance in clinical tirals. 

Dr. Pang earned her master degree from Sun Yet-sen University, Guangzhou, Guangdong, China, major in oncology in 2005. She joined our company in Jan, 2021.

Publications

• Biomarkers in head and neck squamous cell carcinoma: unraveling the path to precision immunotherapy

Martine Poelman, MD, is an Executive Medical Director, Oncology, for Fortrea, based in Brussels, Belgium. She provides medical and scientific support to help advance drug development in hematological malignancies for Fortrea clients. Dr. Poelman brings more than 30 years of experience in clinical research and development as a physician and medical director, specializing in pediatrics and oncology, to Fortrea. Before assuming her current position, she served more than 15 years as Global Head of Oncology Research for Fortrea, providing medical monitoring for more than 200 clinical trials. Before joining Fortrea, she served as Clinical Research Physician, Hemato-Oncology-Infectiology, for Eli Lilly in Brussels. Before going into research, she served as Bone Marrow Transplantation and Hemato-Oncology Physician for the Department of Pediatric Oncology, Wilhelmina Children’s Hospital, in The Netherlands. Martine joined our company in November 1996.

Publications

• The Evolving Landscape in Multiple Myeloma: From Risk Stratification to T Cell-Directed Advanced Therapies
• Mechanisms of immune modulation in the tumor microenvironment and implications for targeted therapy

María García Requesens, MD, is a Medical Director at Fortrea based in Madrid, Spain. Dr. García has 5 years of experience in oncology clinical drug development clinical trials in pharma and CROs. She focuses on medical support of global oncology clinical trials for solid tumors. Dr. García earned her medical degree from Universidad Europea in Madrid. She also holds a Nursing Degree and is very patient-oriented, believing in the power of cross-functional communication. She joined Fortrea (formerly Labcorp) in January 2020.

Yulianna Tymovska, MD, PhD, is Senior Medical Director based in Brisbane, Australia. Dr. Tymovska has 20 years of clinical experience, specializing in Oncology (extensive clinical experience in breast, head and neck cancer, melanoma, and gynecology malignancies diagnostic and treatment, as well as research in mechanisms of tumors resistance to anti-cancer treatment and immune oncology). 

Dr. Tymovska has more than 15 years of clinical research experience as a clinical trial investigator and medical director (monitor) providing medical expert oversight and monitoring of clinical trials, contribution and scientific expertise to study design, and regulatory documents, work in cross functional team on all phases of the studies and trials including feasibility assessments, design process, education efforts, and management of medical information. 

Dr. Tymovska earned her medical degree and completed clinical oncology postgraduate training in Bogomolets National Medical University, Kyiv, Ukraine, and PhD training in Kavetsky IEPOR of NAS of Ukraine. She joined our company in Jan 2023.

Liang Wan, MD, PhD, is a Medical Director for Fortrea in Shanghai, China. He serves as lead project physician on clients’ drug development projects, provides medical/scientific expertise to project teams, reviews protocols and medical data, and is responsible for medical and safety monitoring on assigned projects. 

Dr. Wan has more than 25 years of experience as a physician, research clinician and medical director with therapeutic experience in oncology, gastroenterology, and hematology. Before joining Fortrea, he was Medical Director for IQVIA in Shanghai, serving as Global or Regional Medical Advisor on assigned projects. He began his career as a surgeon and clinical investigator at Shanghai Jiao Tong University Rui Jin Hospital. Dr. Wan joined our company in May 2019.

Reigetsu Yoshikawa, MD, PhD, is a Senior Medical Director for Fortrea in Osaka, Japan. She contributes to the development of medical strategies and execution of clients’ clinical programs and provides medical/scientific expertise to project teams. Dr. Yoshikawa has more than 30 years of experience as a physician, medical director/advisor, and professor of medicine in Japan. 

Before joining Fortrea, she was Senior Medical Advisor for Eli Lilly and previously served as Senior Medical Lead for Dainippon Sumitomo Pharma in Japan. Dr. Yoshikawa has served on the editorial boards of several peer-reviewed journals and has authored or co-authored dozens of articles, presentations, and abstracts. She joined our company in January 2021.