Aegis Technology Solutions
Aegis Technology Solutions is a global provider of end-to-end services in the Pharmaceutical, Biotechnology, and Medical Devices industries. They specialize in Biometrics, Data Management, Validation, Drug Safety, Regulatory Affairs, and Pharmacovigilance. Their mission is to combine superior technical knowledge with integrity and dedication to deliver exceptional service, insight, and world-class execution. Their vision is to deliver innovative and effective technology solutions that make a difference in their clients' businesses and the lives of their customers. They aim to meet the expectations of excellence for clients, employees, candidates, and the community, continuously satisfying the world's evolving demand for technology.
Industries
Nr. of Employees
small (1-50)
Aegis Technology Solutions
Products
Aegis Technology Solutions Functional Service Provider and Contract Staffing Services
End-to-end services in the Pharmaceutical, Biotechnology, and Medical Devices industries specializing in Biometrics, Data Management, Validation, Drug Safety, Regulatory Affairs, and Pharmacovigilance.
SAS Programming Services
Professional SAS programming services for clinical trial data analysis in pharmaceutical, biotech, and clinical research companies, providing study summary tables, data listings, and graphs.
Validation Services
Validation process and consulting establishing documented evidence that a specific process consistently produces products meeting predetermined specifications, complying with GxP and SOX requirements.
Clinical Data Management Services
Professional services for collecting and managing clinical research data in accordance with regulatory standards to generate high-quality, reliable, and statistically sound data from clinical trials.
Medical Affairs
Comprehensive medical affairs services encompassing strategy, safety, communications, post-launch trials, field teams, therapeutic training materials development, and training management.
pharmaceutical regulatory affairs consulting
Professional consulting services for navigating regulatory requirements, acting as a liaison between industry and government, and ensuring compliance for pharmaceutical products.
Aegis Technology Solutions Functional Service Provider and Contract Staffing Services
End-to-end services in the Pharmaceutical, Biotechnology, and Medical Devices industries specializing in Biometrics, Data Management, Validation, Drug Safety, Regulatory Affairs, and Pharmacovigilance.
SAS Programming Services
Professional SAS programming services for clinical trial data analysis in pharmaceutical, biotech, and clinical research companies, providing study summary tables, data listings, and graphs.
Validation Services
Validation process and consulting establishing documented evidence that a specific process consistently produces products meeting predetermined specifications, complying with GxP and SOX requirements.
Clinical Data Management Services
Professional services for collecting and managing clinical research data in accordance with regulatory standards to generate high-quality, reliable, and statistically sound data from clinical trials.
Medical Affairs
Comprehensive medical affairs services encompassing strategy, safety, communications, post-launch trials, field teams, therapeutic training materials development, and training management.
pharmaceutical regulatory affairs consulting
Professional consulting services for navigating regulatory requirements, acting as a liaison between industry and government, and ensuring compliance for pharmaceutical products.
Services
End-to-end clinical data management services for clinical research projects.
Statistical programming support for clinical trial data analysis and report generation.
Regulatory support services covering documentation and regulatory strategy.
Validation services providing documented evidence that processes or systems meet specified requirements.
Medical affairs support for scientific communication and clinical lifecycle activities.
Safety monitoring and pharmacovigilance services for adverse event management and reporting.
End-to-end clinical data management services for clinical research projects.
Statistical programming support for clinical trial data analysis and report generation.
Regulatory support services covering documentation and regulatory strategy.
Validation services providing documented evidence that processes or systems meet specified requirements.
Medical affairs support for scientific communication and clinical lifecycle activities.
Safety monitoring and pharmacovigilance services for adverse event management and reporting.
Expertise Areas
- Clinical trial management
- Clinical data management
- Biostatistics and statistical programming
- Pharmacovigilance and drug safety
Key Technologies
- Clinical data management systems (CDMS)
- Statistical programming (e.g., SAS)
- Pharmacovigilance/safety databases
- Data standards for clinical data
News & Updates
Our client is looking for an Associate Director of Biostatistics responsible for directing biostatistics activities for clinical studies, including trial design, execution, analysis, and data interpretation.
The Clinical Data Standards Manager is a key role on the Data Science team, leveraging industry-leading data assets and analytical models to transform the clinical development industry.
Our client is looking for an Associate Director of Biostatistics responsible for directing biostatistics activities for clinical studies, including trial design, execution, analysis, and data interpretation.
The Clinical Data Standards Manager is a key role on the Data Science team, leveraging industry-leading data assets and analytical models to transform the clinical development industry.