Despite the impact on women’s health worldwide, significant unmet needs exist in the diagnosis and treatment of gynecologic cancers. Located in the female reproductive system, many have a reputation for being “silent,” as they are often detected in later stages when treatment options are limited.
However, the recent introduction of novel medicines — targeted therapies in particular — has led to improvements in patient care and uncovered new research opportunities, creating a competitive research environment. With investment in research on the rise, investigators face challenges in patient identification, site selection, and an ever-changing regulatory landscape.
Join Premier Research experts for this webinar on the challenges and opportunities within gynecologic cancer research.
(Moderator) Mary Gunn, Ph.D., COO, Women's Health and Diagnostics, Premier Research
Dr. Mary Gunn is a senior-level scientist with more than two decades of clinical development experience. Dr. Gunn has led development programs through various steps in the R&D lifecycle, from preclinical development to post-approval marketing. She has served as a senior strategist for large and small pharmaceutical, biotechnology and diagnostics companies supporting large, global healthcare programs in women’s health, autoimmune disorders, and oncology.Message Presenter
Rupa Doshi, Ph.D., Vice President, Program Strategy, Oncology, Premier Research
Rupa Doshi is an Executive Director, Oncology at Premier Research. With more than 23 years in the industry, Rupa is an experienced professional with demonstrated leadership skills in clinical operations, global project/program management, customer management and strategy development. Her experience spans the clinical development spectrum from pre-IND to NDA, and she has also led global teams in the execution of full-service complex clinical trials across all phases.
Rupa brings drug discovery and clinical development experience with biologics, small molecules as well as cell and gene therapy products over a range of indications. Her doctoral research focus was on breast cancer, her post-doctoral research was in site-directed mutagenesis, and she holds patents in the area of angiogenesis. Rupa has also supported three products resulting in agency approval.Message Presenter
Andrew Berchuck, M.D., Medical Advisor, Gynecologic Oncology, Premier Research
Dr. Andrew Berchuck is Director of the Duke Division of Gynecologic Oncology and holds the James M. Ingram Distinguished Professorship. As a practicing oncologist, he is actively involved in surgical and chemotherapy management for women with ovarian, endometrial, and lower genital tract cancers. Dr. Berchuck also leads research efforts focused on the molecular-genetic alterations involved in the malignant transformation of ovarian and endometrial epithelium.Message Presenter
Irene Figari, Vice President, Regulatory Strategy, Premier Consulting
Irene Figari brings 40 years of biotech experience to the Premier Consulting regulatory affairs team. She spent 16 years in basic research and development, focusing on immunology, cell biology, tumor model systems, and molecular biology, then moved to the regulatory side in roles of increasing responsibility and leadership. She led a team of regulatory professionals in providing strategic and tactical guidance across therapeutic areas and disciplines in the clinical; nonclinical; and chemistry, manufacturing, and controls arenas. She has also provided regulatory leadership and strategy development for products from the pre-investigational new drug (IND) stage through post-marketing in multiple therapeutic areas, with a focus on oncology.Message Presenter
Who Should Attend?
This webinar will benefit managers and above at biotech and specialty pharma companies with job functions including, but not limited, to:
- Clinical Operations
- Medical Affairs
- Project Management
- Regulatory Affairs
What You Will Learn
Join this webinar for a panel discussion of:
- Current trends in maintenance therapy
- The use of biomarkers for patient selection
- Program planning considerations
- Regulations and the FDA perspective
Premier Research, a clinical research company, is dedicated to helping biotech, specialty pharma, and device innovators transform life-changing ideas and breakthrough science into new medical treatments. As a global company, Premier specializes in the use of innovative technologies for smart study design and trial management to deliver clean, conclusive data to sponsors. Whether it’s developing product lifecycle strategies, reducing clinical development cycle times, securing access to patients, navigating global regulations, maximizing the impact of limited rare disease data, or providing expertise in specific therapeutic areas, Premier is committed to helping its customers answer the unmet needs of patients across a broad range of medical conditions. Visit premier-research.com.
You Must Login To Register for this Free Webinar
Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.Create Account