Kolabtree connects businesses to freelance clinical trial consultants from all over the world.
With expertise in industries ranging from healthcare to manufacturing, our qualified experts are available on demand.
Life science, biotech and medical device organisations use Kolabtree to find experts who can help with scientific writing, product development, research and analytics.
Our freelancers are present in over 170 countries and work remotely on your project using our in-platform workspace. We take extra steps to protect your confidentiality and safety. Our 100% satisfaction guarantee assures you of a safe, secure and risk-free experience.
Clinical trial consulting
Kolabtree’s specialists are PhD-qualified and have decades of experience in academia and research. Having worked for leading organisations and universities in the life sciences sector, our experts provide support with the end-to-end spectrum of clinical research functions.
Our experts are specialists in a wide range of therapeutic areas and scientific disciplines, including but not limited to:
- Genetics and genomics
- Infectious diseases
Our clinical research consultants support a variety of projects from organisations of all sizes.
Medical writing services
Our experts can help you write, edit and review clinical study reports, clinical trial protocols, grant writing (National Institute of Health Small Business Innovation Research (NIH SBIR), for example), clinical evaluation reports for medical devices, institutional review board (IRB) documents, statistical analysis plans (SAPs) and more.
Many of our experts also offer scientific content writing services for authoritative white papers, blogs and sales brochures.
Statistical and regulatory consulting services
Our statistical consultants and freelance biostatisticians provide support for study design, sample size optimisation, statistical analysis, predictive modelling and verification of research data.
Kolabtree’s freelance regulatory writers can help you develop robust technical documentation required for regulatory approvals.
Whether you need help with the Food and Drug Administration’s (FDA) New Drug Application or 510(k) submissions or European Union Medical Device Regulation (EU MDR) compliance, our experts ensure you comply with all requirements.
Clinical trial consultant benefits
While large companies traditionally outsource clinical research services to a contract research organisation (CRO), many small companies may not have the budget to do so.
Hiring experts on demand is a cost-effective, efficient way to access talent on a limited budget without compromising on quality.
Outsourcing clinical research functions that can be performed remotely, such as technical / regulatory documentation and statistical analysis, are of particular benefit to small businesses.