About Clariscript

I am a freelance consultant based in Cheshire, UK, with extensive experience (over 15 years) in the pharmaceutical and contract research industry.

I founded Clariscript Communications Ltd to provide services in medical writing, project management and consultancy on clinical trial transparency requirements to the bioscience industry.

I have extensive experience in providing expert communications leadership for global crossfunctional project teams to generate high quality clinical-regulatory documents. This spans early phase clinical development through to life-cycle management.

Additionally, I offer expertise in non-clinical drug discovery and development, particularly Drug Metabolism and Pharmacokinetics.

I have also worked in a client-facing environment, authoring non-clinical reports and managing numerous projects for a wide variety of international clients. I possess an excellent understanding of the needs of the customer, obtained through wide-ranging experience in both the pharmaceutical and contract research industries.

I was the AstraZeneca business lead for redactions and a core team member of the AstraZeneca Clinical Trial Transparency Taskforce since its inception. I was integral to building business processes and training materials for redactions.

I have strong knowledge of EMA Policy 0070, including how this is constantly evolving, and how this impacts the medical writing community going forward. I was a member of the TransCelerate CSR subteam, providing me with a wide view of the industry.

For the range of services offered please see services.

Please feel free to contact us to discuss your requirements.