Consultant Real-World Evidence & Medical Affairs
IQVIA
Join a great team to accelerate innovation for a healthier world!We are looking for an enthusiastic Consultant Real-World Evidence and Medical Affairs with a scientific background and a lot of natural curiosity to join our Real-World Evidence (RWE) and Market Access team. We are recruiting a consultant to be based in Amsterdam with the objective to contribute to the development and execution of leading international Real-World Evidence studies, and in addition to contribute to value-based healthcare initiatives. The ideal candidate will be an experienced (3-6 years) epidemiologist, researcher and/or consultant with a strong methodological background.With our multidimensional solutions and offerings, we are dedicated to accelerating innovation for a healthier world, together with various stakeholders in healthcare. This includes but is not limited to pharmaceutical, consumer health, and MedTech companies, national and local governments, healthcare insurance companies, hospitals, patient organizations, and academic partners. To increase our impact on healthcare, we would like to strengthen our Real-World Evidence department and are therefore looking for a passionate consultant with a curious and data driven mindset. Passion for improving healthcare and having a societal impact is a plus.Our team has a strong presence within the IQVIA the Netherlands organization and our Amsterdam office and consists of over ten professionals with different backgrounds and expertise, such as: real-world data, medicine, epidemiology, health technology assessment, health economics, pharmaceutical sciences, and data analytics. There are lots of opportunities to develop your own ideas in collaboration with a diverse and talented group of coworkers and to connect with colleagues in- and outside of work.Tasks and responsibilitiesAs a consultant, you will be responsible for the execution and/or project management of our client projects under the supervision of Senior Healthcare Consultants and/or Associate Directors. You will contribute to the development of study designs and protocols as well as the execution of real-world evidence studies. You will be in direct contact with our clients, write briefings to our teams and translate research results in high-quality deliverables such as clinical study reports and peer-reviewed manuscripts. Your work environment will be fast-paced and complex, requiring you to balance projects across various disease areas, using a range of methodologies and working in rotating project teams. At IQVIA, you will be given the opportunity to develop broader and deeper knowledge of epidemiological methodologies and medical writing, and will be exposed to a wide variety of disease areas.As a member of our team your responsibilities will include:
Required knowledge, skills & abilitiesFormal qualifications and experience
Specific skills and abilities
LocationBased at our office in Amsterdam Zuid-Oost with the flexibility to work from home. You will join client meetings F2F or virtually.What is in it for you?
Career opportunities at IQVIAIf the above-mentioned role does not match with your professional aspirations, please consult our job pages to discover other vacancies and apply, or join our Talent Network:IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Amsterdam, Noord-Holland
Sun, 22 Sep 2024 05:44:57 GMT
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