Job Title: Clinical Research Associate II (CRA II) Location: Germany (Travelling 6-8 times per week)
The Clinical Research Associate II (CRA II) is responsible for independently monitoring clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements. The CRA II acts as the primary point of contact for investigative sites and plays a key role in ensuring data integrity, patient safety, and timely study execution.
German regulatory authorities such as BfArM/PEI)
Verify source data and ensure accuracy, completeness, and consistency of clinical trial data
Maintain regular communication with investigators and site staff
Support site training and ensure proper study documentation and filing (e.g., Track study progress and provide regular status updates to project teams
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field
~2–4 years of CRA experience in clinical trials (monitoring experience required)
~ Fluent in German and English (written and spoken)
~ Effective communication and interpersonal skills
Competitive salary and benefits package
Flexible working arrangements (home-based options)
Career development and training opportunities
International and collaborative work environment