Clarity Contracts provides a specialist service to pharmaceutical and biotechnology companies in the management, negotiation and processing of contracts with clinical trial sites

Template Preparation

Our experience in country template preparation will advance your clinical trial start-up process by ensuring templates are readily available for submission packages and distribution to clinical trial sites

Centralized Experience

With our centralized experience in the management, negotiation and processing of contracts with clinical trial sites, we can help you to make 'go' / 'no-go' decisions upfront and avoid unnecessary, time-consuming and costly negotiations

Risk Management

Through our centralized review process, we can achieve compliance with your corporate risk management strategy when negotiating contracts with clinical trial sites

Planning and Management

Our experience in upfront planning, prioritization and ongoing management during the start-up phase of a clinical trial will expedite the completion of your site contract process

Our Services

The management, processing and negotiation of contracts with clinical trial sites is often mentioned as one of the reasons causing delay to the start of a clinical trial. The various range of country templates, site specific requirements, as well as templates or signed contracts required for submission packages, means that it is essential to invest time and money upfront to effectively prioritize, plan and manage the diverse requirements of each country as soon as countries and sites are selected.

Clarity Contracts is experienced in contracting with clinical trial sites and understands the common reasons why contracts are delayed. Whether your contracts with clinical trial sites are processed in-house or outsourced to an external vendor, we have developed solutions to improve the delivery of this transactional service during the start-up period of a clinical trial. By improving how contracts with sites are managed and how information during negotiations is retained, contracts with clinical trial sites can be signed in a timely manner and future negotiations simplified.