Advancing Diversity in Oncology Clinical Trials: 5 Key Insights from Clinical Trial Sites
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Headquartered in the United States for over two decades, Precision’s reputation is rooted in the strong and enduring relationships we've cultivated over time. Our strategic collaborations with leading researchers across the United States and Canada, have enabled us to optimally advance even the most challenging clinical development programs.
Our integrated clinical development, biomarker expertise, and regulatory, capabilities seamlessly combine to deliver unique value to our clients through their clinical development journey in the Americas.
Each phase of clinical development requires a unique skill set and expertise. With 50+ global centres of excellence for oncology across the United States and Canada, Precision is well-equipped to drive robust outcomes from early through to late phase development. With the research infrastructure and experience of our network, we craft the boldest approaches to drive even the most complex development programs.
Precision’s track record across the Americas is backed by the successful approval of multiple products supported through the years. We have diligently worked towards being recognized as a partner with top-tier clinical research expertise, assisting you in achieving operational efficiency, providing timely insights for informed decision-making, and ultimately expediting regulatory submissions.
Simon Fleming
Executive Vice President
Sallyanne Williams
Senior Vice President, Global Head Project Management
Nithiya Ananthakrishnan
Senior Vice President, Biometrics
Teresa Pokladowski
Regional Vice President, Clinical Business Solutions, North America
Sheila Antonio
Vice President, Clinical Data Management
With Precision's robust presence across the Americas, you have a strong and unified team to respond to any changes in the clinical and regulatory environment in the course of your development lifecycle.
Navigating your clinical development program from strategic planning through meticulous execution to a successful regulatory submission.
Building agile expert teams across geographies to help you tide over tight development and submission timelines.
Stay ahead with the latest insights from Precision’s team of experts. Discover valuable perspectives, updates, and strategies to achieve expedited trial outcomes across the Americas.
Leverage an integrated infrastructure that reduces the inefficiencies inherent in complex development. Integrate lab and trial execution to increase speed to market. Incorporate manufacturing expertise for advances therapies to ensure scalability. Precision can customize and converge our capabilities for your program's unique needs.
Award-winning CRO with deep oncology and rare disease expertise
Exceptional translational and biomarker sciences with global central lab services
Pioneers in planning, building and maintaining manufacturing at scale for pharma and biotechs.
Explore how Precision for Medicine can help simplify even the most complex clinical programs, throughout the Americas.
Executive Vice President
Veteran of the pharmaceutical industry, fluent in all aspects of clinical trial management, including business development, strategic operations, process improvement, technology implementation and finance. Special focus on global quality management, data management, biostatistics and statistical programming operations.
Senior Vice President, Global Head Project Management
Long-standing project management leader dedicated to improving delivery across all phases of product development. Working on a global scale, applies strategic smarts to operational delivery and financial management. Recognized as one of the PharmaVoice 100, some of the industry’s most inspiring people, awarded in the “Change Agent” category.
Senior Vice President, Biometrics
Visionary executive with a distinguished track-record fostering an environment of continuous innovation and growth through people-centric strategies. Data sciences leader focused on data analysis, visualization, and solutions to solve key issues in clinical trials. On a personal level, deeply committed to supporting educational excellence, particularly for underprivileged children.
Regional Vice President, Clinical Business Solutions, North America
Teresa is a respected business development strategist, building successful clinical programs for clients in Massachusetts. She is an innovator of fresh approaches to biomarker planning, translational solutions, and clinical study design. Her experience spans the execution of Phase 1-4 clinical trials, specialty lab services, companion and in vitro diagnostic strategies, and biomarker data management.
Vice President, Clinical Data Management
Sheila Antonio is the Vice President of Global Data Management at Precision for Medicine. She has more than 25 years of clinical research industry experience in Clinical Data Management. Sheila is well-known as a highly driven technical subject matter expert for managing clinical trial data, SAS programming, and EDC database design and development. She has been a key leader at various contract research organizations (CROs) in developing the mission, values, and strategic goals to create efficient and driven Clinical Data Management teams. Sheila develops programs that focus on thorough technical trainings, as well as effective and positive communications which lead to overall data quality improvements and successful team collaboration.