C-TASC Services

Trial and Study Management

C-TASC has led the design and conduct of clinical trials, cohort studies, cross-sectional studies and case-control studies for over 15 years. Our Professional staff includes MDs, PhD Biostatisticians and MS Statisticians with experience in coordinating all types of studies.   We provide complete research management including study design (medical and statistical), project management,  performance monitoring and data quality control, data analysis, publication and presentation of study findings and contract management. 

Each C-TASC senior staff member has from 10 to 30 years of experience in designing, implementing, and reporting the results of clinical studies including design and implementation of large multi-center studies involving thousands of subjects. 

Hourly consultation services are available for study design, study conduct and data analysis. C-TASC also has its own Institutional Review Board to assist you in reviewing your study with respect to subject safety, privacy and record confidentiality.

C-TASC Specialties 

• CANCER 
• CARDIOVASCULAR DISEASE
• AIDS 
• PULMONARY DISEASES
• CYSTIC FIBROSIS 
• PHARMACO-EPIDEMIOLOGY 
• BIO-RESPOSITORY ESTABLISHMENT & COORDINATION
  

Technology

Our cutting edge Technology Services group is available to support all studies with database and application design and development for both web based and client server based data management systems that are fully HIPAA compliant.

C-TASC maintains a state-of-the-art data center to safely and securely store and manage all critical study data and to provide the most advanced statistical modeling possible using SAS and other advanced statistical tools.

We also offer consulting services for data management, data security and system design.