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Home >

Power of Partnerships Series: Sites Weigh-in on the New Normal with DCTs

 
$79.00 (Non-Member Price)
$0.00 (SCRS members – Included as member benefit, no additional cost)

Not an SCRS member? Join now to attend this webinar at no additional cost.

Date and Time: September 20, 2022 @ 12:00 PM ET

Contact Hours: One contact hour will be issued.
Contact Hours are not available for archived webinars.


Sponsored by Medidata


Presenter:

Kelly McKee, VP, Patient Registries and Recruitment, Medidata (Moderator) 
Phyllisa DeRoze, Patient Advocate
Taryn Collett CCRC, VP, Clinical Operations and Quality Assurance, Meridian Clinical Research
Gretchen Goller, Seagen


Description:
A site’s role in a DCT is crucial - they are the frontline for patients and play many roles: trainer, helpdesk, protocol consultant, etc. Have you wondered what has changed for sites conducting DCTs since 2020? Medidata has the details on the ways technology usage has increased in the last two years and the changes sites still want to see to streamline decentralization. This webinar provides a summary of data on DCTs collected from sites within the SCRS community in 2020 and 2022.

Join this session to learn about:

  • 1. Challenges sites face when participating in hybrid or decentralized trials.

  • 2. Solutions implemented at sites over the past two years to streamline DCTs.

  • 3. Benefits of incorporating remote elements into trials for sites and patients.


Speaker Bios:

Kelly McKee, VP, Patient Registries and Recruitment, Medidata 

Kelly McKee is the Vice President of Patient Registries and Recruitment at Medidata with 20 years of experience in clinical trial operations, patient recruitment, and innovation. She is a proven clinical trial leader and trailblazer in operationalizing global patient-focused solutions across organizations including innovations in clinical trial awareness, access, and improvements in patient experiences. Kelly is passionate about celebrating the role that clinical trial participants bring in making new medicines and vaccines possible and was named one of PharmaVoice’s 100 Most Inspiring Leaders in 2020, Centerwatch’s Top 20 Innovators of 2018, and PharmaTimes’ Clinical Researcher of the Year, Clinical Research Teams, in 2012.


Phyllisa DeRoze, Patient Advocate

Phyllisa Deroze is a global diabetes patient advocate and Director of Research at dQ&A. She began blogging almost immediately after being diagnosed with type 2 diabetes in 2011. A year later she founded Black Diabetic Info, a website dedicated to increasing awareness of cultural-competent diabetes information from around the African Diaspora. In 2019, after becoming extremely ill, she learned that she had been misdiagnosed with type 2 diabetes for eight years and was finally given the correct diagnosis — Latent Autoimmune Diabetes in Adults, a form of type 1 diabetes. Considered one of the most prolific writers on the representation of diabetes in African American literature and popular culture, Phyllisa builds community through storytelling by drawing on a Ph.D. in English Literature from Pennsylvania State University, a ten-year career as a university professor, her Fulbright Scholar expertise, and her own experiences living with diabetes. In 2021, she returned home to South Florida with her husband and daughter after living abroad in the United Arab Emirates and Martinique for seven years. 

Her motto "Diagnosed Not Defeated" is an inspiration for all.


Taryn Collett, VP, Clinical Operations and Quality Assurance, Meridian Clinical Research

Taryn began her career at Meridian Clinical Research as a coordinator in 2014, quickly becoming a site director for an internal medicine research clinic in Savannah, GA. She has overseen the opening of 14 research sites across the US covering numerous therapeutic specialties including neurology, dermatology, urology, plastic surgery, internal medicine and pediatrics since 2015. Throughout 2020 and 2021, Taryn supported the conduct of COVID-19 vaccine trials at several Meridian sites. The company has enrolled more than 8,000 participants into COVID-19 vaccine trials, including studies for vaccines that were granted Emergency Use Authorization by the FDA. Collett earned a Bachelor of Arts in psychology from Georgia Southern University in 2011, and became a Certified Clinical Research Coordinator in 2016. Taryn is currently responsible for the operations of 9 research clinics in two states, as well as the operations of the Quality Assurance program at Meridian Clinical Research.

 

Gretchen Goller, Seagen, Senior Director, Head of Patient Recruitment Solutions at Seagen

Gretchen Goller leads the Patient Recruitment and Retention Solutions group at Seagen with a focus on oncology-specific solutions resulting in a holistic, patient centered approach ensuring that patients and their families have the most positive experience. Ms. Goller has over 20 years experience gained in pharma and CRO industries. Prior to Seagen, she was the Global Head of the Patient Recruitment and Retention team at ICON and at PRA Health Sciences. Previously, Ms. Goller was the Patient Recruitment and Retention leader at sanofi-aventis. Other roles included Clinical Trial Manager, Medical Affairs at Wyeth and Study Manager at Astra Zeneca. She has held positions at the University of Pennsylvania including Study Coordinator and Site Director working on a range of therapeutic areas including vaccines, cardiovascular, cardiology, ophthalmology, women's health, HIV, and endocrinology. Ms. Goller has a BA from the University of Massachusetts and an MSW from the University of Pennsylvania and is located outside of Philadelphia, PA.




Society for Clinical Research Sites, Inc. is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation.

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To obtain your Contact Hours for this webinar:

  1. The webinar must be watched in its entirety.
  2. The post webinar survey immediately following this webinar must be completed in its entirety.
  3. Your contact hour certificate will be sent to you within 30 days of you viewing this webinar.
  4. The contact hour certificate will be sent to the email address provided when you registered.

Planners, presenters, faculty, authors, and content reviewers do not have any relevant financial relationships with any commercial interest.

This webinar does not imply any endorsement of products or services by the Society for Clinical Research Sites or ANCC.

The materials and recording of this webinar will be available for one year as an archive, but will not award any contact hours.


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