Clinical Trials Associate

This is a fully remote position, open to applicants in Argentina, +2 more states.

📋 Description

• Deliver administrative support and assist in project tracking for the clinical project team.

• Ensure that assigned project tasks related to Project Delivery services are completed promptly and with precision.

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

• Maintain and conduct quality audits of project portal documents to guarantee the latest revisions are in place.

• Aid in the preparation and distribution of clinical trial documentation, which includes Investigator Site Files.

• Oversee version control and quality assurance of project documentation.

• Submit project documentation to the trial master file.

• Monitor and maintain information pertinent to the project, including the site medical question-and-answer log.

⛳️ Requirements

• Exceptional written and spoken English skills.

• Proficiency in the primary language of the country where the position is located.

• Capability to manage multiple tasks while exercising independent judgment.

• Keen attention to detail and a commitment to the quality of work.

• Strong organizational and problem-solving abilities.

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

• A degree-level qualification or equivalent experience is required.

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

• Skill sets and proven performance that align with the above requirements.

🏝️ Benefits

• A diverse and inclusive work environment.

• Supportive and collaborative teams.

• Accessible and hands-on leadership.

• Equal employment opportunities for all.

• Exceptional experiences for employees.

• A workplace that emphasizes collaboration and creativity.