As clinical development becomes increasingly complex and costly, biotech and pharmaceutical companies are rethinking how they partner with contract research organizations (CROs) to harmonize speed, cost, internal bandwidth and project scope. Rather than accepting rigid full-service and functional service provider (FSP) models, many are exploring more flexible hybrid approaches to strike the right balance for their unique needs.
In this webinar, the featured speaker will explore how operating models in clinical development are evolving and what should truly drive the model design for a Sponsor. Using a “soundboard” framework, this webinar will examine how to dial key priorities up or down and understand the trade-offs across full-service, FSP, and hybrid models. Through real-world scenarios, the speaker will highlight how hybrid models work in practice, empowering attendees to rethink the RFP process and approach CRO partnerships more strategically by asking the right questions early.
Register for this webinar to gain practical insights into designing fit-for-purpose operating models that are in tune with clinical development goals and set up clinical programs for success.
Speaker
Cheryl Silva, Vice President, Functional Services, Premier Research
Cheryl Silva is a global clinical research leader and department head who drives the design and delivery of flexible, fit-for-purpose operating models that align resources, expertise and technology to meet client and study needs. With more than 20 years of experience across the clinical research and medical software industries, she leads operational excellence, process optimization, resource allocation and team workflows to increase efficiency and quality. She is passionate about developing talent, fostering collaboration and creating an environment where both her team and clients succeed.
Cheryl has also contributed to industry publications and conference presentations on study start-up, data management and functional outsourcing. Cheryl graduated with honors from UMASS Dartmouth with a Bachelor’s Degree in Computer and Information Science.
Message PresenterWho Should Attend?
This webinar will benefit Managers and above at biotech and specialty pharma companies with job functions including, but not limited, to:
- Drug Development
- Clinical Operations
- Medical Affairs
- Regulatory Affairs
- Project Management
What You Will Learn
Attendees will gain insights into:
- Available operating model options when partnering with flexible contract research organizations
- Key elements to consider in the clinical trial RFP process
- Real-world examples of hybrid models in successful clinical programs
Xtalks Partner
Premier Research
Premier Research International LLC (Premier) is a global leader in clinical research and consulting services with expertise in driving an efficient and effective path to market for the life sciences industry.
Premier is built with the needs of biotech in mind, turning breakthrough science into life-changing drugs, devices, and diagnostics by addressing trial complexity, overcoming development hurdles, and demonstrating product value.
Leveraging deep therapeutic expertise, innovative technology, and product development operational proficiency—from preclinical planning to clinical trial execution and commercialization—our integrated approach offers personalized, end-to-end solutions to identify the pertinent data and insight necessary to make informed decisions earlier and deliver accelerated development timelines for a smarter, faster path to approval. To learn more visit premier-research.com.
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