The key to a successful clinical trial program is spending as much time as possible on upfront planning. A clinical project management approach allows Sponsors to focus on the planning Phase, resulting in fewer delays, unforeseen issues, and errors while ensuring timely execution and high-quality data.

We offer a variety of clinical research services that bring together our global clinical and regulatory expertise with proprietary technologies to simplify your journey to market. The benefit for you is reduced development costs while minimizing risks of late phase failure. Our team provides the comprehensive clinical development services you need, from First-in-Human through Phase IV and Post-marketing surveillance. We also have the regulatory expertise, clinical trial operations management, payer and market access planning, medical education and communications capabilities to see your journey through efficiently and effectively.

Our clinical project management model provides you with a single point of contact to support all your clinical trial needs. Through a true partnership, our Project Managers will work with you to delineate clear roles, responsibilities, and timelines while managing costs. Project Managers will also help develop the project plan and timeline, oversee study start-up, and conduct monitoring, vendor management, data management, and deliverables to get you results on time and on budget.

We bring together the right people, skills, and scientific acumen to provide you with a tailored clinical trial design appropriate to your research goals and commercialization plan. From the outset, we will partner with you to design your clinical trial based on current regulatory and industry knowledge.

Our Clinical research services include:

• Site Selection
• Monitoring
• Data Management
• Medical Writing
• Regulatory Affairs