C3 Research Associates is a quality-focused clinical research development and management group supporting innovative biotechnology, medical device and pharmaceutical organizations, stewarding therapeutics from preclinical through phase IV drug development and successful market life cycle.
Our full service clinical contract research organisation is the perfect choice for small and mid-sized biotechnology, medical device and pharmaceutical companies who are looking for an alternative to working with a traditional large CRO; C3 Research Associates offers all of the same services without the inefficiencies of a big company.
C3 Research Associates partners with our clients; working closely with them through the product development process, responding and adapting quickly if challenges arise. C3 Research Associates can tailor all aspects of drug development to optimise client needs and resources.
Where we differ from larger CROs is in our hands-on approach to managing each project. Our smaller size means each client's project is a top priority and will not be lost amongst dozens of others.
We provide personalised attention to every project, large or small. Our leadership team becomes involved and stays involved in the client's project to ensure proper study preparation, implementation and delivery of impeccable results. Our core team has decades of proven expertise plus broad collective experience in the principal areas of clinical research, operations, medical monitoring, data analysis, biostatistics and regulatory oversight, affording our clients consistency of service in a wide range of product development scenarios. With a physician, pharmacist, PhD biostatistician, clinical operations and regulatory specialist, our combined experience spans all facets of clinical development.
Clinical protocol design, trial management, clinical data management
Examples of our services include clinical protocol design, investigational site selection and monitoring, regional staff placement of clinical research professionals, trial management, clinical data management, biostatistical analysis and medical writing services with regulatory affairs support, evaluation of study reports as well as preparation of materials to be submitted to regulatory agencies (e.g. Food and Drug Administration). Our services extend over a wide variety of diseases including oncology, infectious diseases, rheumatology, neurology and cardiology with experience in broad aspects of therapeutic drugs and medical devices.
We make an uncompromising commitment to client satisfaction, by being thorough, responsive and nimble as the needs of the client and project evolve. With this personalised attention given to each of our clients, C3 Research Associates is dedicated to encouraging innovation while helping our clients achieve their goals.
Clinical research services
C3 Research Associates offers a full range of clinical research services without the inefficiencies, communication challenges and additional costs of a traditional CRO.
C3 Research Associates services:
- Protocol development
- Clinical trial management
- Field monitoring/clinical research associates
- Exploratory IND, Phase 0 Studies
- Medical monitoring
- Clinical and regulatory staffing
- Clinical data management
- Data monitoring committee support
- Medical writing
- Preparation of an FDA New Drug Application (NDA), Abbreviated New Drug Application (ANDA), or Biologics License Application (BLA)
- Quality Assurance
- Regulatory Compliance
2311 North 45th Street, #266
Seattle, Washington 98103