A professional regulatory medical writer for 25 years with 30 years’ experience in the clinical research arena.

A passion for presenting information in a readily accessible way appropriate to the target audience.

A service providing 100% quality control checks.

Clinical study reports, safety narratives, clinical study protocols, informed consent forms, and investigator's brochures prepared to a high standard of quality and accuracy.

Wide experience in the pharmaceutical industry and contract research organisations.

Ducan Currie

I am a UK–based freelance medical writer offering medical writing services to the pharmaceutical and healthcare industry. I undertake to enable my clients to reach their medical writing goals by supplying quality medical writing documents at the required speed and at a competitive price. I strive to create strong and trusting relationships with my clients to ensure that their requirements are satisfactorily met.

I take great pride in my ability to present complex scientific material accurately and clearly.
I focus on putting myself in the reader's place to present information in a readily accessible way highlighting the appropriate key messages to form valid and concise conclusions.

My 25 years of medical writing experience coupled to a clinical pharmacology background enables me to bring a wealth of knowledge and perspective to a wide range of medical writing projects. My speciality is regulatory medical writing, particularly clinical study reports but also safety narratives, clinical study protocols, informed consent forms, summary documents, and related documentation. I am available to undertake quality control work.

Experience

Maze House Medical Ltd

2011 to date

PPD

2008 to 2011

Quanticate

2007 to 2008

Pfizer

1997 to 2007

PRA International

1996 to 1997

H Lundbeck

1995 to 1996

HPRU, Surrey University

1991 to 1995

Clinical Pharmacology Dept. Dundee University

1985 to 1991

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Services

  • Independently written clinical study reports produced for a wide range of therapeutic areas across all drug development phases in accordance with the appropriate regulatory guidelines, SOPs, and style. Clinical study report synopses also written for public disclosure.

  • Compilation of clinical sections of the Common Technical Document.

  • Writing of the full range of regulatory safety narratives to any level of detail as required for clinical study reporting.

  • Protocol writing services for clinical studies of any scope or size and indication following appropriate regulatory requirements, SOPs, and style. I can also update existing protocols with protocol amendments as appropriate.

  • New or updated investigator’s brochures written according to requirements, collecting and compiling up to date information from the relevant suppliers.

  • Informed consent forms for clinical studies produced in a writing style appropriate for the study and the target audience.

  • A comprehensive service ensuring document accuracy, consistency, and coherence and 100% quality control checks against source documents and style needs as appropriate.

  • Organisation of material for scientific papers and abstracts for peer reviewed journals and production of posters for scientific or medical conferences and related destinations.

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