
Clinical Research Associate I / Clinical Research Associate II
Posted May 24

Posted May 24
This is a fully remote position, open to applicants in France.
• Oversee and take ownership of the advancement of clinical trials at research sites.
• Ensure that clinical trials are performed, documented, and reported according to the protocol, standard operating procedures (SOPs), ICH-GCP guidelines, and all relevant regulations and standards.
• Facilitate all essential activities required for the setup and monitoring of a study (e.g., identifying investigators, assisting with regulatory submissions, conducting pre-study and initiation visits, etc.).
• Degree in life sciences and/or equivalent professional experience.
• At least 1 year of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or the pharmaceutical/biotech industry, or relevant experience and/or proven competencies.
• Strong communication and organizational skills are crucial. Must be a collaborative team member.
• Proficiency in English, and for countries where English is not the primary language, fluency in the local language is required.
• Health insurance coverage.
• Flexible working arrangements.
• Opportunities for professional development.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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