Full-Time Clinical Research Associate / Senior CRA

As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.Office-based in Munich/Planegg or Home-based in Germany

You will:

1. Conduct and report all types of onsite monitoring visits as well as remote visits.
2. Perform CRF review, source document verification and query resolution.
3. Be responsible for site communication and management.
4. Be involved in site identification process.
5. Assist in training of less expert CRAs, depending on your level of experience.
6. Senior CRA can be assigned as Lead Monitor in some projects, while still partially monitoring.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• Independent on-site monitoring experience in Germany.
• Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
• Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus.
• Full working proficiency in German, English and MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel and valid driver’s license.

What is the last date for applying to the job?

Which countries are accepted for this remote job?