Clinical Trial Management in the US: Local Service, Global Reach


SGS delivers clinical trials with high-quality data across the Americas and Europe. Our comprehensive clinical trial management services offer you tailored solutions and global coverage with local knowledge.

SGS helps you bring new therapies to market safely and quickly through experienced staff, efficient and accurate feasibility and optimized start-up timelines – with a flexible, customer-focused approach.

With over 40 years of experience as a full-service contract research organization, we provide a wide range of integrated services across the USA – from drug development consultancy activities to Phase I-IV trial management,  as well as bioanalytical and QC testing. We offer unrivaled expertise in international project management and clinical monitoring, and we operate a global network of therapeutic-specific key opinion leaders, subject-matter experts and pre-qualified investigator trial sites. We also provide regulatory guidance and regulatory IND/NDA submission experience in the USA, Canada and Europe, along with expertise in drug import regulations and procedures for every country in Europe and North America.

Contact us to learn more about our clinical trial management solutions:


Strategic Development

Strategic Development

Medical Writing

Medical Writing



Pharmacovigilance and Drug Safety Services

Pharmacovigilance and Drug Safety Services

Regulatory Affairs

Regulatory Affairs

Clinical Pharmacology Unit

Clinical Pharmacology Unit

Laboratory Services

Laboratory Services

Clinical Trial Management

Clinical Trial Management (Phase I-IV)

Feasibility Services

Clinical Study Feasibility Services

SGS Clinical Trial Management

Our flexible clinical trial management solution provides you with:

  • Strategic, data-driven feasibility which allows fast, easy access to patient groups
  • A robust and systematic approach to clinical site evaluation and selection, using local feasibility experts
  • An extensive global network of therapeutic-specific key opinion leaders, subject-matter experts and pre-qualified investigator trial sites
  • Experienced customer-focused project managers, based across Europe and North America
  • Comprehensive site management and quality-focused clinical monitoring 
  • An international network of highly qualified and trained local CRAs
  • Medical monitoring and pharmacovigilance
  • Regulatory guidance and a dedicated team of regulatory affairs experts in place for 70 countries, including the US
  • Integrated CTMS and eTMF on an industry-leading platform
  • Integrated data cleaning, analysis and reporting in collaboration with our biometrics team
  • Medical and regulatory advice for clinical development plans and study protocol designs

Supplementary Asset

Clinical Operations Brochure

Download now

Case Studies

Unrivaled Experience

Group of companies

+500 employees and a network of over 400 investigational sites


+1000 clinical trials executed


Supporting Top 10 Pharmaceutical companies

Data Analysis

+20 therapeutic areas with special focus in infectious diseases and vaccines, respiratory diseases, oncology and CNS/Psychiatry

Audit certification

+400 trials executed at our 88-bed SGS Clinical Phase I Unit

Training Experts

97% recruitment goal achieved

Follow us on LinkedIn

Join the scientific community, connect with SGS on LinkedIn.

Follow Us
Colorless Gas
Contact Us