*CRA or Senior CRA (m/w/d) - sponsor dedicated, office- or home-based in Austria*
Are you interested in collaborating with leading pharma companies to help patients all around the world?
In our Clinical Functional Service Partnership models, we work in a close partnership with key customers in order to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single pharma client and gain direct and in-depth experience of collaborating with this sponsor.
Beside establishing strong relationships with the client and the involved investigators, you will conduct monitoring on complex clinical trials and assure the adherence to good clinical practices, standard operating procedures, and study protocols.
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
We believe in hiring the best clinical talent in the industry.
Applicants should have:
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
At least one year of on-site monitoring experience
Alternatively, you should have an equivalent combination of education, training and experience
Fluent written and verbal communication skills including good command of German and English language (at least C1 Level)
Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Knowledge of applicable protocol requirements as provided in company training
Availability to travel 40-60% of the working time
What you can expect:
Resources that promote your career growth
Leaders that support flexible work schedules
Programs to help you build your therapeutic knowledge
Dynamic work environments that expose you to new experiences
Home-office, company car, accident insurance and more
Salary starting from 50000 EUR brutto yearly, depending on experience
Due to the international scope of our business please apply with English version CV and your certificates and reference letters.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
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