Chimera Clinical Management
A boutique CRO offering scalable, individualized and comprehensive solutions for clinical trial support.
Who We Are
Chimera Clinical Management is a clinical research consulting company offering a full range of services to global biotech, pharmaceutical, and device companies.
Chimera Clinical Management offers turnkey solutions for global project management, document management, regulatory oversight, and both traditional and electronic Trial Master File creation and maintenance.
Chimera Clinical Management provides full study life-cycle support designed to meet the needs of companies looking for high-quality, efficient, and agile clinical trial solutions.
Our unique clinical trial management system provides secure real-time support specifically designed for use by remote and diverse clinical teams. Our common operating methodology ensures open and secure communication, controlled and reliable document access, retention of institutional knowledge, and maximum efficiency.
In addition to clinical trial support services, Chimera Clinical Management also provides quality system build services, including SOP creation and revision, GxP auditing services, corporate training classes, and much more.
What We Do
Our project management team has 50+ years of combined clinical research experience in drug, device, and other pathways. Our therapeutic areas of expertise are broad, including:
Therapeutic Area Experience:
- Cardiovascular Disorders
- COVID-19
- Crohn's Disease
- Diabetes
- Endocrine Disorders
- HIV/AIDS
- Infectious Diseases
- Influenza
- Movement Disorders
- Multiple Sclerosis
- Nuetraceuticals
- Oncology
- Ophthamology
- Organ Transplant
- Respiratory Diseases
- Somatopause
- Vaccines
- Weight Loss