Clinical Trials Associate

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

📋 Description

• Offer administrative and project tracking assistance to clinical project teams

• Ensure that assigned project tasks are completed promptly and with precision

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

• Maintain and conduct quality audits of documents on project portals

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

• Oversee version control and quality assurance of project documentation and submit it to the trial master file

• Monitor and retain project-related information, such as site medical question and answer logs

⛳️ Requirements

• Exceptional written and verbal communication skills in English

• Proficiency in the local language of the country of employment

• Capability to manage multiple tasks while exercising independent judgment

• Keen attention to detail with a strong focus on quality

• 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 position

• Skill sets and proven performance that meet the above criteria

🏝️ Benefits

• Diverse and inclusive workplace environment

• Supportive and cohesive teams

• Accessible leadership

• Equal employment opportunities

• Employee experiences focused on respect and inclusion