Homebased in Canterbury, Kent, United Kingdom, Tracy brings over 25 years of biomedical science and medical writing experience. Tracy provides senior direction and decision making to a global team of medical writing professionals who deliver document development services across the spectrum of peri- and post-approval studies, and strategic writing services including study documents, manuscripts, publication planning, and posters. Tracy is responsible for staffing, high quality document delivery to clients, and the financial performance of her team. Tracy also specializes in data transparency and anonymization providing internal and external expertise. Tracy is the co-chair of the EMWA Regulatory Public Disclosure Special Interest Group and is an active contributor to EMWA and DIA.
Prior to joining Evidera, Tracy was employed by Evidera’s parent company, PPD. Her roles included senior director, director, and associate director with operational responsibilities over clinical medical writing teams. Prior to joining the medical writing group at PPD, Tracy served as a manager of medical writing services for ClinTec International Ltd. While there, she established new global medical writing teams in the United Kingdom, Germany, and India. Earlier in her career, she worked at Pfizer Global Research and Development as a medical writing therapeutic area lead for oncology, central nervous system, allergy, and respiratory, and as a quality and compliance manager for safety data management; Shell Research Ltd in toxicology, and as an analytical chemist and at the National Health Service pathology laboratory.
Tracy received her GI Biol in Biochemistry and higher national certificates in hematology from Bromley College of Further and Higher Education and in chemistry from Canterbury College in Canterbury, Kent.