In-House Clinical Research Associate I - Poland - Remote

Worldwide Clinical Trials is a global, midsize CRO dedicated to pushing boundaries and innovating to improve lives through clinical research. We are seeking a motivated In-House Clinical Research Associate I to join our team in Poland and contribute to our mission of driving scientific breakthroughs.

Key responsibilities

• Ensure the quality and timely submission of data from study sites, including appropriate reporting and follow-up for safety events.
• Compile and maintain regulatory and ethical submission documentation, such as IRB approvals, informed consent forms, and lab certifications.
• Manage site-related documentation and ensure all records are accurately filed in the Trial Master File (TMF).
• Conduct feasibility studies and site identification activities to support clinical trial planning.

Requirements

• Strong interpersonal, oral, and written communication skills with a professional customer-focused approach.
• Proven ability to contribute effectively to a team in a fully remote environment.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Educational background in life sciences or equivalent experience in clinical research, such as a study coordinator or clinical trial assistant role.
• Fluency in English and Polish, plus proficiency in one additional language (German, French, Italian, or Spanish).

What we offer

• The opportunity to work with a global team of experts on innovative clinical trials.
• A supportive, inclusive, and collaborative work environment that values diversity.
• Professional growth within a midsize CRO that prioritizes employee development and success.