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Power of Partnerships Series: Raising Site Voices: The Future of Clinical Research Depends On It

 
$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: October 25, 2022 @ 12:00 PM ET

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

Sponsored by Medidata


Presenters:

Tina Mincher, Director, Client Engagement
Tim Galvin, Director, Product Management, Medidata
Mike Barrera, Senior Director Product Management, Medidata


Description:
 The reality of a clinical trial is what happens at the site.  This makes the site’s feedback extremely valuable and very necessary.  Raising the site's voice in the industry is a huge priority for Medidata and we are here to report back trends and solutions based on data and feedback received during our engagement with sites over the last year.

Join this session to learn about:

  • The latest financial hurdles and solutions that help sites stay financially secure. 
  • Data management & EDC practices that set sites up for success.
  • Streamlined document management and end-of-study media processes that keep sites compliant.     


Speaker Bios:

Tina Mincher, Director, Client Engagement

Tina Mincher is Director of Client Strategy for the suite of Clinical Trial Financial Management products at Medidata Solutions. She has spent 15 years working in the Pharmaceutical sector in client engagement dedicated to all areas of global cost benchmarking, feasibility and analytics center of excellence. Finding innovative solutions on how to elevate the customer experience is a passion for Tina, her favorite phrase being ‘Delight the customer at every interaction.  Tina lives in Canterbury, England with her husband Daniel, daughter Lottie, and Cockerpoo Lundy and thoroughly enjoys family time, going to the theatre, and reading a good book.  


Tim Galvin, Director, Product Management, Medidata

Tim is the Director of the Regulated Content Management platform at Medidata. His role involves the ownership of the products - eTMF, Site Cloud: End of Study, and Archive. He previously worked as a Senior Engagement Consultant at Medidata focusing on eTMF, End of Study Media, Grants Manager, and Payments. He has been in the clinical research space for over 17 years. Tim spent most of his clinical career working in Trial Management, TMF Services, Software Implementation, and Project Management. He has worked at PPD, RPS, PRAHS, and Transperfect. His role has been overseeing the in-house CRA support team, TMF Management, Study Start-Up, and Feasibility.  His roles have been focused on the successful delivery of the clinical services provided to clients with oversight specific to Project Management, TMF Audit readiness, Implementation/Configuration, and TMF Document Review Processing.


Mike Barrera, Senior Director Product Management, Medidata

Mike Barrera has 30 years of experience with clinical development technology and operations within the Life Science space.  He is currently Senior Director, Product Management with the Rave Study Conduct Platform technology.   Mike has been with Medidata for nearly 16 years, primarily in customer-facing roles, and came from a similar position at Oracle where he developed strategies and presented study conduct software solutions to all sectors of the market.  Prior to that Mike has held various data management operational positions for pharma, small and large biotechnology, and CRO organizations.  His career has allowed him to see clinical technology platforms and processes evolve over the past several decades to what is available today, as he helps develop modern capabilities for the future.

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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