Clinical Research Associate - Germany (with sign-on bonus)
RemoteGermany
Job Summary
Conduct independent site visits for pre-study, initiation, interim monitoring, and closeout to ensure compliance, enrollment, and study understanding. Independently perform CRF reviews, generate and resolve queries, and identify retraining opportunities for site personnel. Prepare corrective and preventive action plans, manage EC submissions and document translations, and negotiate study budgets with investigators. Administer site payments and proactively follow CAPA resolutions until timely completion. Requires 2–3 years of clinical trial monitoring experience, fluency in English and German, and a valid driver's license. Sign-on bonus and performance incentives included.
Required Qualifications
- University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
- At least 2 - 3 years of independent clinical trial monitoring in a CRO/pharma
- High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
- Fluent in local language and English, both written and verbal
- Computer proficiency is mandatory
- Ability to read, analyze, and interpret common scientific and technical journals
- Excellent verbal and written communication skills
- Very good interpersonal and negotiation skills
- Ability to work independently, pro-active
- Affinity to work effectively and efficiently in a matrix environment
- A current, valid driver's license
Desired Qualifications
- Preferably in the northern part of Germany
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