Clinical Trials Associate

This is a fully remote position, open to applicants in Mexico.

📋 Description

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

• Organize and monitor system access for the project team members, including Project Managers, Lead CRAs, and CRAs.

• Ensure the maintenance and quality auditing of documents to guarantee that the latest revisions are available on project portals.

• Assist the project team in preparing and shipping clinical trial documentation, such as the Investigator Site File.

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

• Support the tracking and maintenance of project-related information, including the site medical question and answer log.

⛳️ Requirements

• A degree-level qualification or equivalent experience, along with at least one year of experience in a related role.

• Proficient written and verbal English skills, as well as fluency in the local language of the country.

• Capability to manage multiple tasks while exercising independent judgment.

• Strong attention to detail with a focus on delivering high-quality work.

• Excellent organizational and problem-solving abilities.

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

🏝️ Benefits

• Flexible working arrangements.

• Opportunities for professional development.

• A diverse and inclusive work environment.