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Precision Americas CRO Services

Collaborez avec les meilleurs chercheurs. Réalisez vos essais avec précision.
Chez Precision, la recherche innovante fait partie de notre ADN et c'est ce qui nous distingue vraiment dans l'industrie. Grâce aux services de CRO de Precision pour les Amériques, vous avez accès aux institutions de recherche et aux experts les plus éminents du monde, réputés dans leur domaine. Quelle que soit la complexité du projet, nous nous engageons à atteindre votre objectif, à savoir fournir des traitements innovants qui répondent aux besoins non satisfaits des patients, de manière plus efficace et plus intelligente que jamais.
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Precision Americas CRO Services - Pionnier de la recherche de pointe

Basée aux États-Unis depuis plus de vingt ans, la réputation de Precision est ancrée dans les relations solides et durables que nous avons cultivées au fil du temps. Nos collaborations stratégiques avec des chercheurs de premier plan aux États-Unis et au Canada nous ont permis de faire progresser de manière optimale les programmes de développement clinique les plus difficiles.

Nos capacités intégrées de développement clinique, d'expertise en matière de biomarqueurs et de réglementation se combinent de manière transparente pour offrir une valeur unique à nos clients tout au long de leur parcours de développement clinique dans les Amériques.

Gouvernance du FSP

Une réputation fondée sur la réussite et la précision

Les antécédents de Precision dans les Amériques sont étayés par l'approbation réussie de multiples produits soutenus au fil des ans. Nous avons travaillé avec diligence pour être reconnus comme un partenaire disposant d'une expertise de premier plan en matière de recherche clinique, vous aidant à atteindre l'efficacité opérationnelle, à fournir des informations opportunes pour une prise de décision éclairée et, en fin de compte, à accélérer les soumissions réglementaires.

20 Bureaux dans les Amériques
2350 Des experts dans toute la région
5 Des laboratoires de précision pour un développement clinique intégré

L'équipe Precision au service de votre réussite sur le continent américain

  • Simon-Fleming

    Simon Fleming

    Executive Vice President

  • SallyAnne Williams

    Sallyanne Williams

    Executive 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

Des modèles rationalisés pour un environnement en constante évolution

Grâce à la forte présence de Precision sur le continent américain, vous disposez d'une équipe solide et unifiée pour répondre à tout changement dans l'environnement clinique et réglementaire au cours du cycle de vie de votre développement.

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    FSP_Suivi clinique

    Externalisation complète

    La gestion de votre programme de développement clinique, de la planification stratégique à l'exécution méticuleuse, jusqu'à la présentation d'une demande d'homologation réussie.

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    Externalisation complète

    La gestion de votre programme de développement clinique, de la planification stratégique à l'exécution méticuleuse, jusqu'à la présentation d'une demande d'homologation réussie.

    Explorer
  • Explorer
    Precision FSP Managed Solutions

    Précision FSP

    Mise en place d'équipes d'experts agiles dans différentes zones géographiques pour vous aider à respecter des délais de développement et de soumission très serrés.

    Explorer

    Précision FSP

    Mise en place d'équipes d'experts agiles dans différentes zones géographiques pour vous aider à respecter des délais de développement et de soumission très serrés.

    Explorer

Découvrez les dernières idées des experts de Precision

Gardez une longueur d'avance grâce aux dernières informations fournies par l'équipe d'experts de Precision. Découvrez des perspectives, des mises à jour et des stratégies précieuses pour accélérer les résultats des essais dans les Amériques.

Read: Case Study: Delivering an Early-Phase Autoimmune Trial Across Regions Case Study: Delivering an Early-Phase Autoimmune Trial Across Regions

Clinical Trials - Early Phase Research - Autoimmune

Case Study: Delivering an Early-Phase Autoimmune Trial Across Regions

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    has third author: false, (SizeLimitingPyMap: {main={hs_id=214928090133, hs_child_table_id=0, hs_updated_at=1781285625399, hs_published_at=1781630742683, description=Deborah Spencer is a Senior Director of Project Management at Precision for Medicine with over 25 years of experience in clinical research. She specialises in leading global clinical trials across multiple phases, with deep expertise in complex study delivery. Deborah provides strategic oversight of programmes, leads high-performing teams, and partners closely with sponsors to ensure successful execution and regulatory readiness., avatar=Image{width=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Deborah%20Spencer.jpg',altText='Deborah Spencer',fileId=214838919278}, lastname=Spencer, hs_initial_published_at=1781285742914, hs_created_by_user_id=26433386, hs_created_at=1781285562019, hs_is_edited=false, hs_deleted_at=0, name=Deborah, job=Senior Director, Project Management, slug=deborah-spencer, hs_updated_by_user_id=26433386}, second={hs_id=214928170660, hs_child_table_id=0, hs_updated_at=1781285676367, hs_published_at=1781630742683, description=Anthea Gates is a Project Director with approximately 30 years of drug development and medical device industry expertise across all phases, over a variety of indications including breast, lung cancer, solid tumors and lymphoma, cutaneous T-cell lymphoma, malignant melanoma, squamous cell carcinoma, rare haematologic disease, autoimmune rheumatology, osteoarthritis, ocular burns, liver cirrhosis, myopia and pre-eclampsia. Committed to delivering quality and passionate about building positive relationships with clients and study teams to promote cohesive business practices and ensure the successful management of projects from start to finish. Anthea holds a proven track record in effective leadership of cross-functional teams across programs of studies, to the accomplishment of operational excellence., avatar=Image{width=372,height=546,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/profile.jpg',altText='profile',fileId=214846873938}, lastname=Gates, hs_initial_published_at=1781285742914, hs_created_by_user_id=26433386, hs_created_at=1781285639221, hs_is_edited=false, hs_deleted_at=0, name=Anthea, job=Project Director, slug=anthea-gates, hs_updated_by_user_id=26433386}, third={hs_id=214928090141, hs_child_table_id=0, hs_updated_at=1781285738567, hs_published_at=1781630742683, description=Claire Delaville is a Senior Project Manager at Precision for Medicine. She brings 18 years of experience across preclinical and clinical research, including more than a decade leading Phase I to IV studies in oncology, rare diseases, and immunology, with direct experience in first-in-human and multicenter oncology trials. Claire is responsible for maintaining study quality through inspection readiness, corrective action planning, and proactive risk mitigation. She also oversees study budgets and vendor performance to support coordinated delivery across functions, drawing on a scientific foundation that includes a PhD in Neurosciences and Neuropharmacology. Based in Paris, France, Claire aligns scientific insight with operational execution to support successful trial outcomes., avatar=Image{width=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Claire%20Delaville.jpg',altText='Claire Delaville',fileId=214838927033}, lastname=Delaville, hs_initial_published_at=1781285742914, hs_created_by_user_id=26433386, hs_created_at=1781285678112, hs_is_edited=false, hs_deleted_at=0, name=Claire, job=Senior Project Manager, slug=claire-delaville, hs_updated_by_user_id=26433386}})
  • Deborah S. avatar Anthea G. avatar Claire D. avatar
  • Deborah S.

    Anthea G.

    Claire D.

Découvrir
Read: Early‑Phase Autoimmune Drug Development: Trial Design, Biomarkers and Statistical Strategies Early‑Phase Autoimmune Drug Development: Trial Design, Biomarkers and Statistical Strategies

Clinical Trials

Early‑Phase Autoimmune Drug Development: Trial Design, Biomarkers and Statistical Strategies

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=213698206365, hs_child_table_id=0, hs_updated_at=1780680681226, hs_published_at=1781630742683, description=Rui F. Duarte‑Lopes is a senior biostatistics leader with over 31 years of international experience across biopharmaceutical, biotechnology, and CRO sectors. He provides strategic statistical oversight, ensuring rigorous, high‑quality, and decision‑focused delivery aligned with sponsor and regulatory expectations. He has more than 12 years of CRO experience supporting Phase I–IV clinical trials and has held roles including Lead Statistician, Project Lead, and Senior Manager. His therapeutic experience includes oncology and autoimmune diseases, notably lupus erythematosus, Crohn's disease and rheumatoid arthritis. Specializing in oncology over the past six years, Rui focuses on advanced solid tumors and early‑phase studies, contributing to study design, interim analyses, and data‑driven decision frameworks., avatar=Image{width=1200,height=1200,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/Rui%20F%20Duarte-Lopes.jpg',altText='Rui F Duarte-Lopes',fileId=213695319705}, lastname=Duarte-Lopes, hs_initial_published_at=1779886328878, hs_created_by_user_id=26433386, hs_created_at=1779886165792, hs_is_edited=false, hs_deleted_at=0, name=Rui F, job=Senior Manager, Biostatistics, slug=rui-f-duarte-lopes, hs_updated_by_user_id=26433386}, second={}, third={}})
  • Rui F Duarte-Lopes avatar

    Rui F Duarte-Lopes

Découvrir
Read: China’s New Drug Regulatory Framework Positions the Country as a Global Hub for Innovative Medicine Launches China’s New Drug Regulatory Framework Positions the Country as a Global Hub for Innovative Medicine Launches

Clinical Trials

China’s New Drug Regulatory Framework Positions the Country as a Global Hub for Innovative Medicine Launches

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    has not third author: true, (SizeLimitingPyMap: {main={hs_id=209983237513, hs_child_table_id=0, hs_updated_at=1774533604788, hs_published_at=1781630742683, description=Calvin Niu received his BD in pharmaceuticals from Lanzhou University. He has brought over 22 years of drug development and regulatory experience in pharmaceutical companies and CROs. Calvin’s regulatory expertise covers regulatory agency engagements and all types of regulatory submissions throughout product development and post market life cycles in oncology, immunology, ophthalmology, clinical nutrition, cardiovascular, gastroenterology, women’s health, CNS, rare disease, etc. , avatar=Image{width=276,height=290,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Calvin%20Niu.png',altText='Calvin Niu',fileId=209991702802}, lastname=Niu, hs_initial_published_at=1774533614867, hs_created_by_user_id=51739740, hs_created_at=1774531720533, hs_is_edited=false, hs_deleted_at=0, name=Calvin, job=Director, Regulatory Affairs, China, slug=calvin-niu, hs_updated_by_user_id=26433386}, second={}, third={}})
  • Calvin Niu avatar

    Calvin Niu

Découvrir

Des capacités spécialisées à chaque étape du développement clinique

Tirer parti d'une infrastructure intégrée qui réduit les inefficacités inhérentes à un développement complexe. Intégrer l'exécution des laboratoires et des essais pour accélérer la mise sur le marché. Precision peut personnaliser et faire converger ses capacités pour répondre aux besoins uniques de votre programme, ce qui favorise l'efficacité, l'agilité et la réussite du début à la fin.

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    soutien aux essais cliniques

    CRO mondial
    Services

    CRO primé avec une grande expertise en oncologie et en maladies rares

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    Services de laboratoire spécialisés

    Laboratoire mondial
    Services

    Des sciences translationnelles et des sciences des biomarqueurs exceptionnelles avec des services de laboratoire central à l'échelle mondiale

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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

Executive 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.