Nienke Flipsen joins Qserve

Nienke Flipsen joins CRO

Our Qserve CRO team is happy to announce that Nienke Flipsen has joined them as Clinical Data Manager.

As Clinical Data Manager, Nienke is responsible for collecting, validating and processing of clinical study data of multiple clinical studies. She also reviews the data quality, and overviews clinical databases. Nienke is based in the Netherlands.

Nienke has a background in medical devices and eHealth. After obtaining her Master degree in Medical Biology, she worked as business researcher, at a startup that developed an online medical platform for people with Chronic kidney disease. After that, she worked in a startup which developed a smartwatch for people with Parkinsons disease. Here she worked on clinical research and pilot studies, but also did QA/RA (ISO 13485) and some business development. Nienke really enjoys the eHealth/medical innovation field, and is looking forward to further explore it at Qserve Group.

Nienke has a Master degree in Medical Biology from the Radboud University in Nijmegen, where she specialized in neuroscience and research, both in humans and animals. Current areas of expertise include neuroendocrinology, neurodegenerative diseases and nephrology. Nienke is also experienced at designing and performing animal trials.


About Qserve Group

Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We guide manufacturers in gaining and maintaining compliance and conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years of combined expertise in the medical field. Teams in the EU, USA, and China provide a global footprint for global regulatory, clinical, CRO, and quality services.

Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs, or auditing in medical devices. Check our current vacancies.

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