Alithia Life Sciences
Australian-owned boutique full-service Contract Research Organization (CRO) providing end-to-end clinical development support for pharmaceutical, biotechnology, medical device companies and institutional research groups. Services cover first-in-human and Phase I–III studies, clinical operations, regulatory planning, data management and biostatistics, site and vendor management, and executive/directorship support for programs conducted in Australia and internationally.
Industries
Nr. of Employees
small (1-50)
Alithia Life Sciences
Products
Clinical Trial Project Management
Management and clinical strategy for Phase I to III clinical trials from concept to close out for pharmaceutical, biotech, and device sponsors.
Biotech Executive Management and Director Support
Provision of executive management and local directorship services for biotech companies involved in clinical research.
Clinical Research Suite
Comprehensive clinical research services including project and site management, site feasibility, vendor selection, monitoring, data management, biostatistics, and medical monitoring.
Identification and Access to Key Opinion Leaders (KOLs)
Services to identify and connect with Key Opinion Leaders relevant to clinical research projects.
Clinical and Regulatory Project Planning and Study Design
Planning and designing clinical and regulatory projects in compliance with international guidance documents.
Access to Project Enabling Vendors
Providing access to a network of vendors including laboratories and R&D tax experts to support clinical research projects.
Clinical Trial Project Management
Management and clinical strategy for Phase I to III clinical trials from concept to close out for pharmaceutical, biotech, and device sponsors.
Biotech Executive Management and Director Support
Provision of executive management and local directorship services for biotech companies involved in clinical research.
Clinical Research Suite
Comprehensive clinical research services including project and site management, site feasibility, vendor selection, monitoring, data management, biostatistics, and medical monitoring.
Identification and Access to Key Opinion Leaders (KOLs)
Services to identify and connect with Key Opinion Leaders relevant to clinical research projects.
Clinical and Regulatory Project Planning and Study Design
Planning and designing clinical and regulatory projects in compliance with international guidance documents.
Access to Project Enabling Vendors
Providing access to a network of vendors including laboratories and R&D tax experts to support clinical research projects.
Services
End-to-end clinical development support for pharmaceutical, biotechnology, device companies and institutional research groups in Australia and internationally.
Clinical program governance, study planning, sponsor representation and operational oversight throughout study lifecycle.
Assessment and selection of investigational sites and ongoing site management to support recruitment and compliance.
Monitoring services and medical oversight for clinical trials, provided locally and for global studies.
Data management services and biostatistical support for study design, analysis and reporting.
Protocol development and regulatory planning aligned to international guidance; support to navigate regulatory pathways.
End-to-end clinical development support for pharmaceutical, biotechnology, device companies and institutional research groups in Australia and internationally.
Clinical program governance, study planning, sponsor representation and operational oversight throughout study lifecycle.
Assessment and selection of investigational sites and ongoing site management to support recruitment and compliance.
Monitoring services and medical oversight for clinical trials, provided locally and for global studies.
Data management services and biostatistical support for study design, analysis and reporting.
Protocol development and regulatory planning aligned to international guidance; support to navigate regulatory pathways.
Expertise Areas
- Clinical trial management
- First-in-human (FIH) and Phase I studies
- Regulatory compliance and study submission planning
- Clinical data management and biostatistics
Key Technologies
- Clinical trial design
- Clinical data management systems
- Biostatistical analysis
- Medical monitoring