Outstanding Project Management. Delivering Excellence.
For every client inVentiv Health Clinical assigns an experienced project manager who is responsible for study oversight. The project manager has the authority to pull together the necessary resources and lead the operational teams in meetings critical milestones and deliverables while ensuring projects stay on time, budget and scope. Team members have a focused specialty in clinical operations and scientific and regulatory affairs to ensure the study will be executed on time and within the scope of the requirements.
The clinical operations team includes a wide range of on-site medical professionals such as doctors, nurses, medical technicians, and clinical research monitors in order to provide the safest environment and accurate results. Our relationships with local hospitals give us access to experienced staff in a variety of specialties including special populations, cardiac safety, and drug interactions, providing support for the most complex clinical trials.
Scientific and regulatory affairs experts collaborate with our sponsors throughout the study on assessment of overall feasibility, protocol development, bioanalytical and clinical feasibility, recruitment planning and screening, institutional review board presentations, and regulatory submission.
From protocol design to development of robust quality and regulatory controls, inVentiv Health Clinical's works with you to execute strategies that minimize risk and promote compliance throughout the study. Quality assurance processes, including internal training programs, vendor audits, software validation, and robust SOPs ensure the highest standards in quality, compliance, and the safety of study participants.