Who are Clariscript?

Debbie Slamon

I am a freelance consultant based in Cheshire, UK, with extensive experience providing expert communications leadership to global cross-functional project teams, spanning early phase clinical development through to life-cycle management. I also provide expertise in non-clinical drug discovery and development, particularly Drug Metabolism and Pharmacokinetics.

I was the AstraZeneca business lead for Redactions and a founding member of their clinical trial transparency taskforce. I have strong knowledge of clinical trial disclosure regulations (EMA Policy 0070) including how this is constantly evolving, and how this impacts both the medical writing community and bioscience industry.

What do Clariscript do?

I am delivery-orientated with a strong understanding of the customer obtained through extensive experience in both the pharmaceutical and contract research environments.

I drive efficiencies by providing a flexible resourcing solution. I work collaboratively with your teams to generate their required outcomes – be this writing high quality documents, providing training and consultancy on clinical trial disclosure or helping your team manage a project to time and quality.

Why Clariscript?

I founded Clariscript Communications Ltd to provide services in medical writing, project management and consultancy on clinical trial disclosure requirements to the bioscience industry. For the full range of services offered please see services or contact me to discuss your requirements further.