Clinical Trials Associate

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

📋 Description

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

• Ensure that tasks associated with assigned projects in Project Delivery services are completed promptly and accurately.

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

• Maintain and conduct quality audits of project portal documents to ensure that the latest revisions are accessible.

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

• Maintain version control and quality of project documentation, submitting it to the trial master file.

• Track and manage project-related information, including the medical question and answer log for the site.

⛳️ Requirements

• Exceptional written and verbal proficiency in English.

• Fluency in the local language of the country where the role is based.

• Capability to manage multiple tasks while exercising independent judgment.

• Strong attention to detail and a commitment to delivering 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 professional experience.

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

• Relevant skill sets and demonstrated performance that meets the above criteria.

🏝️ Benefits

• A diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible leadership.

• Equal employment opportunities for all.

• Opportunities for employees to excel and perform their best work.