What will be your role at Key2Compliance?
I will work in the team of clinical development where I will assist our clients with clinical evaluations and other assignments related to medical devices.
What is your background?
I have a MSc in Materials Chemistry Engineering and I started my journey in industry with 13 years in a tech startup, Scint-X, within x-ray imaging, where I was a part of bringing the company from research, through scale up of processes, and to exit through acquisition. Then I have been almost 3 years at Abilia, where I have had roles as technical project manager, strategic portfolio manager and medical science liaison, working a lot with clinical evaluations, MDR and ISO 13485.
What are you looking forward to the most at Key2Compliance?
I look forward to a lot! Being a part of a great team, working with different types of customers and gain more knowledge in the areas we are working within.
What will be your role at Key2Compliance?
I will provide professional help to IVD and MD companies with their regulatory questions and needs in order to be able to understand, write, and update their technical documents and other regulatory related tasks.
What is your background?
I have double master’s degree in Molecular Biology and Medical Biotechnology. After graduation from KTH, I worked in a lab at KI and then in an IVD company. Working in a fast-growing start-up company and taking multiple roles over the course of several years enabled me to develop my skills in this field.
What are you looking forward to the most at Key2Compliance?
I am looking forward to meeting new clients and to make a good relation with them while helping them to comply to the regulatory requirements for CE marking but also to learn and develop my skills within the projects. I am also looking forward to work in a competent team with all my smart new colleagues!
What will be your role at Key2Compliance?
I will work as a Clinical Development Consultant within the Clinical Development team.
What is your background?
Most recently as Clinical Coordinator at Barncancerfonden and responsible for Barncancerfondens training programs, grants to pediatric oncology departments and healthcare staff, evaluations, investigations, and initiate meetings with stakeholders to help improve care of children with cancer.
Before I was a Study Coordinator at Karolinska University Hospital conducting clinical trials phase II- III in oncology as malignant melanoma, breast cancer, abdominal cancer and pediatric cancer with immunotherapy and checkpoint inhibitors (ATMP).
What are you looking forward to the most at Key2Compliance?
I am looking forward to using my previous work experience to support customers in clinical investigations, learn all about the monitor role and to be a part of a great team!
Interested in joining our talented and rapidly growing team of specialists? Check out our open opportunities here!
