CLIENT BENEFITS
Courante projects have encompassed all aspects of phase 1, 2, and 3 clinical trials, ranging from initial feasibility studies and protocol development to site monitoring and closeout visits. Also included are writing, editing, or managing reviews of final study reports, serious adverse event narratives, manuscripts, and NDA and IND submissions.
Our Consultants
Courante Oncology consultants complement their clinical research experience with a rich work history including nursing, pharmacy, medical technology, data management, nutrition, statistics, and law. When you choose Courante, you tap into our collective expertise.
Consistency
Courante consultants are personally dedicated to oncology product development, which reflects in low turnover rates and consistent staff assignments throughout the life of a project.
Flexibility
Clients can select the service(s) that benefit any phase of their product development process.
Cost Effectiveness
Our consultants are independent contractors. This allows us to provide services without significant overhead.
Personalized and Efficient Service
Our size allows us to focus our efforts so we can respond to clients’ needs and timelines. Our network of experienced, regionally based CRAs reduces travel costs and provides site support when and where it is needed. Our collaborative, team approach enables us to provide a premium product to our clients.
Accelerated Study Start-up
Access to our established contacts with U.S. and international investigators ensures rapid study start-up.
Experience
Our consultants, including CRAs, medical writers, and contract negotiators, have extensive clinical research experience with a specific focus on oncology-related indications.
Our Consultants
Courante Oncology consultants complement their clinical research experience with a rich work history including nursing, pharmacy, medical technology, data management, nutrition, statistics, and law. When you choose Courante, you tap into our collective expertise.
Consistency
Courante consultants are personally dedicated to oncology product development, which reflects in low turnover rates and consistent staff assignments throughout the life of a project.
Flexibility
Clients can select the service(s) that benefit any phase of their product development process.
Cost Effectiveness
Our consultants are independent contractors. This allows us to provide services without significant overhead.
Personalized and Efficient Service
Our size allows us to focus our efforts so we can respond to clients’ needs and timelines. Our network of experienced, regionally based CRAs reduces travel costs and provides site support when and where it is needed. Our collaborative, team approach enables us to provide a premium product to our clients.
Accelerated Study Start-up
Access to our established contacts with U.S. and international investigators ensures rapid study start-up.
Experience
Our consultants, including CRAs, medical writers, and contract negotiators, have extensive clinical research experience with a specific focus on oncology-related indications.