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Precision Americas CRO Services

Collaborate with the best-in-class researchers. Execute your trials with Precision.
At Precision, pathbreaking research is part of our DNA and what truly distinguishes us in the industry. Through Precision's Americas CRO services, you gain access to the world’s most prominent research institutions and experts who are globally renowned in their fields. Regardless of the complexity involved, we are dedicated to achieving your objective of delivering innovative treatments that meet unmet patient needs, more efficiently and intelligently than ever before.
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Precision Americas CRO Services- Pioneering cutting-edge research 

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.

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A reputation built on success and precision

 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.

20 Offices across the Americas
2350 Experts across the region
5 Precision labs for integrated clinical development

The Precision team driving your success in the Americas

  • Simon-Fleming

    Simon Fleming

    Executive Vice President

  • SallyAnne Williams

    Sallyanne Williams

    Senior Vice President, Global Head Project Management

  • Nithiyanandhan-Ananthakrishnan-1

    Nithiya Ananthakrishnan

    Senior Vice President, Biometrics

  • Teresa-Pokladowski-300x300

    Teresa Pokladowski

    Regional Vice President, Clinical Business Solutions, North America

  • Sheila-Antonio

    Sheila Antonio

    Vice President, Clinical Data Management

Streamlined models for an ever-changing environment

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.

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    Full-Service Outsourcing

    Navigating your clinical development program from strategic planning through meticulous execution to a successful regulatory submission.

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    Precision FSP

    Building agile expert teams across geographies to help you tide over tight development and submission timelines.

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Explore the latest insights from Precision’s experts

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.

 

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Clinical Trials

Case Study Phase 3 NSCLC: Site Relationships Streamline Feasibility

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    Anna Rodecki
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Read: Source Data Verification Types, Trends, and Tips Source Data Verification Types, Trends, and Tips

Clinical Trials

Source Data Verification Types, Trends, and Tips

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=183222587782, hs_child_table_id=0, hs_updated_at=1732630460690, hs_published_at=1739807653319, description=Jelena Alexander brings 18 years of industry experience across the CRO, biotech and R&D arenas, with the last eight years focused on clinical operations oversight and aligning resources with project needs. Prior to transitioning to clinical research, Jelena obtained a Master’s degree in infectious disease and immunology, specializing in the development of cross-reactive and neutralizing monoclonal antibodies to foot-and-moth disease virus. Jelena is a collaborative leader recognized for fostering relationships with stakeholders to embed sustainable workflow processes and for delivering high quality outputs to ensure business needs are accomplished on time and within budget. Jelena’s expertise extends to evaluating and assessing clinical proposals, with a focus on monitoring strategies, and operational feasibility. In this role, Jelena leverages operational and leadership expertise to deliver high-quality, client-focused solutions while enhancing efficiency and sustainability in proposal strategies. Jelena is devoted to driving innovation, mentoring teams, and achieving results through adaptability and commitment to quality., avatar=Image{width=800,height=800,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Jelena%20Alexander.jpg',altText='Jelena Alexander',fileId=183228271491}, lastname=Alexander, hs_initial_published_at=1732630470588, hs_created_by_user_id=26433386, hs_created_at=1732630317363, hs_is_edited=false, hs_deleted_at=0, name=Jelena, job=Senior Manager, Global Clinical Monitoring, slug=jelena-alexander, hs_updated_by_user_id=26433386}, second={}, third={}})
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    Jelena Alexander
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Read: How to launch a clinical trial in South Korea: Investigational New Drug Application Process How to launch a clinical trial in South Korea: Investigational New Drug Application Process

Clinical Trials - Regulatory

How to launch a clinical trial in South Korea: Investigational New Drug Application Process

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    MeeHyun B.
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    Helen O.
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Specialized capabilities in every stage of clinical development

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.

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    Award-winning CRO with deep oncology and rare disease expertise

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    Global Laboratory
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    Exceptional translational and biomarker sciences with global central lab services

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    Manufacturing

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    Pioneers in planning, building and maintaining manufacturing at scale for pharma and biotechs.

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Simon-Fleming
Simon Fleming

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.
SallyAnne Williams
Sallyanne Williams

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.
Nithiyanandhan-Ananthakrishnan-1
Nithiya Ananthakrishnan

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.
Teresa-Pokladowski-300x300
Teresa Pokladowski

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.
Sheila-Antonio
Sheila Antonio

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.