Maria Kołtowska-Häggström, a medical director at Proper Medical Writing – is a specialist in medical and regulatory writing.
With more than 20 years’ experience in senior positions within global pharmaceutical companies (Senior Medical Director at Pfizer Inc.), she has been involved in the design of clinical trials, including observational studies and patient registries, and she has actively taken part in the preparation of clinical trial documentation.
Maria has been a leading member of numerous research groups investigating patients with pituitary disorders managed in real-life clinical settings. Furthermore, she has an extensive track record in research relating to quality of life and patient-reported outcomes. She is a member of various professional societies; in particular she is an active member of the European Medical Writing Association (EMWA) in which she is a workshop leader and a member of the editorial board of Medical Writing.
