Clinical Trials Associate, EMEA

This is a fully remote position, open to applicants in Czechia, +1 more country.

📋 Description

• Provide support for administrative tasks and project tracking to clinical project teams.

• Ensure that all assigned Project Delivery services tasks are executed in a timely and accurate manner.

• Organize and monitor system access for members of the project team.

• Maintain and conduct quality audits of documents in the project portal.

• Assist in the preparation and distribution of clinical trial documentation, including the Investigator Site File.

• Oversee document version control and ensure quality standards are met.

• Submit project documentation to the trial master file.

• Track and manage project-related information, including logs of medical questions and answers from sites.

⛳️ Requirements

• Exceptional written and spoken English proficiency.

• Fluency in the language spoken in the country of employment.

• Capability to manage multiple tasks while exercising independent judgment.

• Strong attention to detail and a commitment to high-quality work.

• Excellent organizational and problem-solving abilities.

• Proficient in MS Office applications, including Outlook, Word, Excel, and PowerPoint.

• Degree-level qualification or equivalent experience is required.

• At least one year of experience in a related position.

• Skill sets and proven performance on par with the aforementioned requirements.

🏝️ Benefits

• Equal employment opportunities for all, regardless of protected characteristics.

• A diverse and inclusive workplace culture.

• Supportive and collaborative team environment.

• Accessible leadership.

• Opportunities for employees to succeed and thrive.