We are committed to providing the best clinical research professionals available to help our clients bring critical products to market. Impact Clinical can quickly identify and allocate experienced resource professionals to meet our clients’ unique requirements. We maintain a resource pool of clinical trial experts including clinical trial managers, medical writing professionals, regulatory consultants, and medical monitors. Whether the need is for an individual contributor or an entire project team, our clients rely on and trust our expertise to provide the personnel they need to conduct their trials with integrity. Our highly skilled team will work with you to develop resourcing solutions that meet your needs and objectives and closely partner with you to ensure success.
All IMPACT employees are trained in industry best practices and our SOPs. We provide the ultimate in quality control with the ability to meet your rapid and aggressive timelines.
Because of our large pool of experienced project managers, we assign a dedicated PM with extensive knowledge of the therapeutic area, the specific indication and often even the therapeutic approach you’re investigating.
No levels, no layers, no A or B teams – every consultant at Impact is a valuable contributor.
Strategic partnerships to extend your team.
When considering a strategic collaborator in your drug development process, you need a trusted partner who can serve as an extension of your team. From the development of an individual molecule to the support of an entire portfolio, we support a wide range of goals. At impact, partnership management is a critical competency that we deliver to unlock greater value for our strategic partners.
As your strategic partner, we we build a close, collaborative relationship with you to understand your project deliverables and build cost-savings into a efficient development model. Find out how we can help accelerate timelines and maximize value.
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