With more than 13 years in the pharmaceutical industry working mostly with drug safety and medical affairs, I have a solid understanding of drug development and in particular medical affairs. My experience includes planning the communication and publication strategy of clinical data resulting in scientific presentations at international conferences, preparing and presenting scientific data to both internal and external stakeholders, performing medical compliance review of scientific and promotional materials and co-authoring several publications.
There is an increasing demand and importance of clear and consistent communication to healthcare professionals. With MedLink I want to support biotech- and pharmaceutical companies with clinical data presentation to external and internal stakeholders, publication planning, medical compliance review of scientific and promotional materials as well as other needs within communication and dissemination of clinical data to relevant stakeholders. Get in touch to discuss your needs and what I have to offer to support you with your communication and to reach your goals.
I deliver high-quality documents on time and on budget.
These services can be tailored to your needs either on a stand-alone basis (small or large) or as an integrated part of a clinical development programme or study.
Get in touch to learn more or to schedule an informal meeting to discuss your needs.
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Last updated March 2021
