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Webinar: Seven Habits of Highly Effective Clinical Research Sites
CINCINNATI, OH — Medpace’s Manager of Patient Recruitment, Betsy Harris, recently co-presented a webinar hosted by TrialJoin.
WEBINAR: Seven Habits of Highly Effective (Clinical Research) Sites
DURATION: 60 MINUTES
ACCESS THE RECORDING HERE
About the Webinar
Delayed enrollment impacts most clinical trials (According to Cutting Edge Information, 72% of studies run more than one month behind schedule).
Slow enrollment into clinical trials is the number one reason for delays in getting new drugs approved.
Patent expirations are not moved out to accommodate delays in drug approvals; meaning that accelerating enrollment into clinical trials enhances the revenue stream from newly launched drugs.
Key takeaways from this webinar:
- A formula for estimating the dollar value associated with accelerating enrollment into a clinical trial
- A novel, cost-effective, customized approach for uncovering and implementing the unique drivers that will accelerate subject recruitment
- The importance of integrating “old world” strategies with technology/social media to enhance recruitment efforts
- Identify ways to optimize your site using tools and tracking methods described
- Develop study specific patient recruitment strategies for outreach outside your clinic’s database
- Build a strong internal and external patient referral network to raise community awareness and increase participation in your clinical studies
About Betsy Harris
Betsy Harris is a Manager of the recently formed Patient Recruitment and Retention Team at Medpace, a mid-size CRO in Cincinnati, OH. She has been a Certified Clinical Research Coordinator since 2000 and has over 27 years of clinical research experience at the site level. She came to Medpace from Sterling Research Group, a dedicated clinical research site, where she worked for 17 years and served as Sr. Project Manager of Marketing and Patient Recruitment for the last 9 years. Prior to that she was a Clinical Research Coordinator on more than 300 trials. She also has experience in academia research and spent 5 years working at Cincinnati Children’s Hospital and 5 years at the University of Cincinnati Lipid Research Clinic at which time she worked on both industry sponsored and NIH funded clinical trials.
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its physician-led, high-science, and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,500 people across 35 countries.