Clinical Trials Associate

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

📋 Description

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

• Ensure and audit project portals to guarantee that the latest document revisions are accessible.

• Support the project team in the preparation and distribution of clinical trial documentation, such as the Investigator Site File.

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

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

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

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

⛳️ Requirements

• Exceptional written and verbal English skills, along with fluency in the local language.

• Capability to manage multiple tasks and make independent decisions.

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

• Excellent organizational and problem-solving abilities.

• Proficiency 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.

• Skills and proven performance consistent with the above requirements.

🏝️ Benefits

• Competitive benefits package based on location.

• Inclusive and equitable workplace environment.

• Transparent compensation and pay equity.