Medpace’s Women’s Health Leadership team brings deep therapeutic expertise and strategic development of women’s health clinical programs to make your study a success.
Medpace’s Women’s Health Leadership team brings deep therapeutic expertise and strategic development of women’s health clinical programs to make your study a success.
Women’s Health CRO for Global Phase I-IV Clinical Trials
Medpace is a full-service CRO supporting women’s health clinical trials across the female health lifecycle.
As women’s health clinical development has become increasingly complex, successful programs require dedicated expertise in study design, endpoint strategy, patient engagement, specialized site networks and navigation of evolving regulatory expectations.
Leverage Medpace’s medical expertise, global regulatory knowledge, operational experience, and cross-functional therapeutic teams to expedite your study start-up times, keep patients engaged, bypass pitfalls, and accelerate the licensing of life-changing therapies.
Making the Complex Seamless® in Global Women’s Health Clinical Trials
The Medpace women’s health team has a deep understanding of the complexity of managing clinical trials in a broad range of conditions. Including but not limited to:
Vulvovaginitis
HPV
Contraceptives
Female Urinary Incontinence
For over 30 years, Sponsors across emerging biotechnology and global pharmaceutical companies have trusted Medpace to lead their women’s health clinical development.
At Medpace, our female-led Women’s Health Leadership team consists of medical and operational experts who possess deep clinical knowledge of Women’s Health indications, study design and execution.
Cross-Functional Support
The intersection of Women’s Health and related diverse disciplines is handled through the collaboration of our medical leadership and functional areas. Medpace accelerates Women’s Health development by fully embedding medical leadership and a wide array of relevant therapeutic expertise, integrated across all functional areas, into the clinical trial process.
By integrating medical leadership across all functional areas, we optimize trial communication and execution, leading to expedited timelines and improved outcomes.
Diverse Therapeutic Execution in Women’s Health
The intersection of Women’s Health and related diverse disciplines is handled through the collaboration of our medical leadership and functional areas. Medpace accelerates Women’s Health development by fully embedding medical leadership and a wide array of relevant therapeutic expertise, integrated across all functional areas, into the clinical trial process. This cross-therapeutic and cross-functional collaboration allows for optimized trial communication and execution, and ultimately, expedited timelines.
Medpace’s Women’s Health CRO Capabilities
When you partner with Women’s Health CRO Medpace, medical leadership is fully embedded within the clinical trial process from inception to completion to help accelerate development.
Ultimately, we at Medpace strive to fill the many unmet needs in women’s health and improve healthcare outcomes and quality of life for women across the globe.
At Medpace, our Women’s Health experts possess extensive expertise in gynecologic and urogynecologic conditions. Our distinguished Women’s Health medical team provide leadership across a wide spectrum of these disciplines, ensuring comprehensive care and innovative approaches. With a combination of deep clinical knowledge and robust research experience, we excel in designing and executing gynecologic and urogynecologic clinical trials.
Our four wholly owned laboratories offer full-service support to six continents for Phase I-IV studies. We have extensive experience in microbiology and virology from small and simple clinical trials to those trials that are large, global, and complex.
Our global laboratory facilities, standardized testing platforms, comprehensive test menu, and stellar project management teams allow Medpace to set up fully customized projects for our clients. Combined with Medpace Clinical Research Organization expertise, we provide a fully integrated solution for your clinical development needs.
Proactive Patient Recruitment & Retention in Women’s Health Clinical Trials
The success of clinical trials is wholly dependent on the success of sites and the engagement of patients. Our proprietary IntelliPACE® feasibility strategy is informed by a multitude of internal and external sources to provide a highly customized, informed recruitment strategy for each study. Accelerate patient enrollment with strategic guidance from our dedicated, in-house patient recruitment and retention teams who are experienced in recruiting complex patient populations.
“Our Women’s Health Leadership Team understands the challenges and opportunities within the field of Women’s Health, and are dedicated to advancing therapies for women globally. Medpace is uniquely positioned to navigate the complexities of Obstetric, Gynecologic, and Urogynecologic clinical development.”
Rujin Ju, MD, MSCR, FACOG Medical Director, Medical Department, Women’s Health
“At Medpace, the intersection of Women’s Health and related diverse disciplines, such as Infectious Diseases and Vaccines, are handled through the collaboration of medical and functional areas. Our combined experience translates into optimal study design and execution.”
Beth Tulip Senior Executive Director, Clinical Trial Management, ID&V and Women’s Health
