As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry and delivering exemplary customer service.
Office-based in Vienna
You will:
- Conduct and report all types of onsite monitoring visits as well as remote visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be involved in site identification process
- Assist in training of less expert CRAs, depending on your level of experience
*Senior CRA can be assigned as Lead Monitor in some projects, while still partially monitoring.
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Austria
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases, Multiple Sclerosis is a plus
- Full working proficiency in English and German
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
We offer:
- Excellent working conditions
- Extensive training and friendly team
- Opportunities for personal and professional growth
- A fair and attractive salary and benefits package starting at EUR 48.000 gross. The actual salary depends on the specific qualification and experience.
