Date posted: September 27, 2019
Location: Vienna, Austria
HOOKIPA Pharma Inc. (NASDAQ: HOOK) is a clinical stage biopharmaceutical company developing a new class of immunotherapeutics, targeting infectious diseases and cancers based on its proprietary arenavirus platform that is designed to reprogram the body's immune system.
HOOKIPA has an open writer position with a focus on pre-clinical, clinical and GMO topics. The Scientist, Pre-Clinical Writer (m/f) will join the Regulatory Affairs team to develop high-quality, scientifically accurate preclinical and clinical communications materials for publication and presentation to a variety of audiences. As a Scientist, Pre-Clinical Writer, you will work collaboratively with the R&D, Clinical and Technical Development teams to analyze data, write, review, edit, and submit scientific, clinical, and regulatory documents for publication. He/she will also work on other technical literature for internal and external use as needed.
As Scientist, Pre-Clinical Writer, you will ideally have a background in molecular biology - Virology, gene therapy, tumor biology. The ideal candidate is a clear and precise writer, detail-oriented, driven, independent, and able to respond quickly to evolving needs. Good analytical and writing skills, ability to work in a fast-paced environment and professionalism are all essential behaviors for this role.
This position within the Regulatory Affairs department will be based in Vienna, Austria.
We are required by Austrian law to post a minimum salary. The minimum monthly gross salary for this position is EUR 3.714,- based on fulltime (40 hours per week); depending on experience and qualification salary can be negotiated. In addition, we offer a performance-related bonus payment and participation in our stock option compensation program.
Starting date: As soon as possible
If you (m/f) are interested in this challenging position, please send your CV including cover letter and credentials to: email@example.com
For more information on HOOKIPA please visit www.hookipapharma.com
Ihr Aufgabenbereich: Umfasst vor allem: Projektmanagement von pädiatrisch hämato-onkologischen klinischen Studien und wissenschaftlichen Teilprojekten, Schnittstelle zu diversen internen und externen Partnern,...
AOP Orphan is a European pioneer in the development, marketing and distribution of medicines for people with rare and complex diseases.To enhance our team in Vienna Headquarters we...
Your responsibilities: Your responsibilities include, but are not limited to: • Performing Trial Monitoring Activities related to initiation and conduct (recruitment, quality data collection) as well as timely completion...