Helping You Expedite the Clinical Trial Process

C3 Clinical Sciences provides expert clinical research consulting services to pharmaceutical, biotechnology and consumer products companies, as well as Clinical Research Organizations.

Learn More About Us

Over the years, we’ve developed a broad network of study monitors who have the expertise you need to effectively conduct your clinical trial. In addition, our network includes project managers, auditors, data managers and biostatisticians, each of whom have the expertise you need to effectively conduct your clinical trial.  C3 Clinical Sciences consistently delivers timely, accurate and complete clinical trial results with steadfast adherence to sponsors’ SOP’s and to ICH/GCP.

What Makes Us Different?

In today’s market, companies face the increasing challenge of proving the safety and efficacy of their products while continuing to strive for efficiency in a competitive industry. C3 Clinical Sciences has the experience, insight and resources to help you expedite your clinical trial process.

Founder and President Ken Canter

Ken Canter, founder and President of C3 Clinical Sciences, is a senior-level clinical research consultant with more than 20 years of hands-on experience in regulatory affairs, clinical monitoring, quality assurance and project management. His level of knowledge and accomplished experience distinguishes him in the clinical research industry. Over the years, Ken has developed an extensive network of seasoned consultants who have continuously and consistently delivered quality and integrity in pharmaceutical, biotech and consumer product development.

C3’s network of consultants delivers a consistently high level of quality by matching the right consultant to the right client project.

C3’s highly trained consultants have the expertise and skill sets necessary to meet the challenges of complex clinical trials.

We blend seasoned management, clinical research expertise and a collaborative approach to ensure integrity and long-term client relationships.

We specialize in building strong relationships with investigators, research nurses, study coordinators and other medical staff to ensure compliance and a successful clinical study.

Our hands-on services and seamless processes result in accurate, objective and timely clinical data reporting.

  • We specialize in:

    • Study Monitoring
    • Project Management
    • Quality Assurance 
    • Data Management
    • Regulatory Affairs
  • Areas of Expertise

    C3 Clinical Sciences provides study monitors, project managers, auditors, data managers and biostatisticians with expertise in many therapeutic areas including, but not limited to:

    • Cardiovascular
    • Cholesterol
    • Central Nervous System
    • Endocrinology
    • Gastroenterology
    • Hematology
    • Immunology
    • Infectious diseases
    • Medical devices
    • Oncology
    • Respiratory
    • Rheumatology