Live opening · Posted 3 days ago

Clinical Research Associate / Senior Clinical Research Associate

PSI CRO · Munich, BY, Germany
Smartrecruiters Hybrid Full-time
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At a glance

The key details from the original listing.

Posted 3 days ago
CompanyPSI CRO
LocationMunich, BY, Germany
Job typeFull-time
Work modeHybrid
SkillsClinical Research
SourceSmartrecruiters
ListedPosted 3 days ago

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About the role

Description supplied by the original job listing.

We are looking for a Clinical Research Associate / Senior Clinical Research Associate to join a highly motivated, international team where collaboration, ownership, and trust are part of everyday work.
Hybrid role in Munich/Planegg or Home-based in Germany
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.
What makes the role different:
Own your studies, not just your visit reports. You will use your managerial skills to take a lead for assigned studies, site strategy, performance, and delivery rather than simply monitoring tasks.
Challenging studies. You will work across multiple sponsors and broad therapeutic areas, keeping your work varied and scientifically engaging.
Focus on quality over quantity. You will work on fewer protocols, enabling deeper study focus and stronger site relationships across Germany nationwide and, where applicable, Switzerland.
You will work on complex and scientifically interesting trials.
Autonomy and trust. We empower our CRAs to make decisions, solve problems, and drive study success.
Collaborative culture. Join a company known for supportive managers, approachable leadership, and teams that genuinely work together.
Long-term career growth. Whether you want to develop broader project leadership skills, we'll support your progression.
College/University degree in Life Sciences or an equivalent combination of education, training & experience.
Independent on-site monitoring experience in Germany. Experience in Switzerland is a plus.
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 professional proficiency in German and English. French / Italian language skills are an asset.
Advanced 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 and valid driver’s license.

Employment type
Full-time

Work arrangement
Hybrid

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