Your team demands talent that’s up to date on the latest regulations, scientific discoveries, and technological advancements in the life science industry. Intego Clinical provides you with just that. We staff top-tier Statistical Programmers, Data Managers, Biostatisticians, and clinical data professionals with an innate drive to stay at the forefront of their fields, and we provide them with the professional development, training and education to feed that drive. This commitment, backed by our company’s history of excellence, quality of service, and proven recruitment and HR processes, ensures you have a valued, long-term partner in your global resourcing strategy.
Intego boasts the largest number of clinical data professionals in Eastern Europe
Intego is a Tier 1 FSP Partner for several of big pharma’s top 10 companies
We are a reliable business partner for Statistical Programming, Data Management, and other professionals in Biometrics because we offer customized solutions supported by superior talent. We service Pharma, CRO, and biotech clients with tailored approaches designed to fit your specific needs, whether that be FSP Staff-Augmentation, Unit-Based, or Full-Service engagement.
Our global market operations are always expanding through our portfolio of training programs in Statistical Programming, Biostatistics, and Data Management, allowing us to grow up to 20% annually and offer unparalleled support to the life science industry.
We provide comprehensive end-to-end services, from Phase I to post-marketing, in all major therapeutic areas, and we comply with all regulatory global standards. Our attention to detail and willingness to problem-solve make us the ideal partner for your clinical studies.
We help our clients get the most out of their clinical data with innovative and accurate data management solutions. Our experienced data specialists are experts in various data collections and reporting systems used throughout Phase I-IV studies.
We’ve successfully brought many drugs in all main therapeutic areas to market over the years. From study conception to analysis and regulatory submissions, we help our clients get the most impact and insights from their clinical studies.
We produce clear and consistent documents for clients at every stage of the clinical development process. Our experienced team of medical writers creates regulatory submissions, patient and investigator brochures, and study reports for clients across all major therapeutic areas.
We bring software engineering talent from different industries to deliver creative solutions in the clinical setting. Our IT experts come from a variety of industries, bringing fresh perspectives to challenges in software development.
We specialize in all aspects of regulatory data compliance and migration strategies. No matter the size and scope of the project, Intego Clinical can map your current or legacy data to all major CDISC formats and advise on adherence to industry standards.
