Clinical Trials Associate

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

📋 Description

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

• Oversee and conduct quality audits of project portals to guarantee the availability of the latest document revisions

• Aid in the preparation and distribution of clinical trial documentation, such as the Investigator Site File

• Manage version control and quality assurance of project documentation

• Submit project documentation to the trial master file

• Track and maintain information related to projects, including logs of medical questions and answers from sites

• Provide administrative support and project tracking assistance to the clinical project team

• Ensure that assigned project tasks are executed promptly and accurately

⛳️ Requirements

• Exceptional written and verbal communication skills in English

• Proficiency 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 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

• At least one year of experience in a related field

• Skills and proven track record comparable to the above criteria

🏝️ Benefits

• A diverse and inclusive workplace

• Supportive teams with accessible leadership

• Equal employment opportunities for all

• Outstanding employee experiences

• Opportunity to collaborate with a global team of over 3,500 experts