Clinical Trials Associate – US/LATAM

Posted 1 day ago

This is a fully remote position, open to applicants in United States, +4 more locations.

πŸ“‹ Description

β€’ Oversee and monitor system access for members of the project team.

β€’ Manage project portals and carry out quality assessments to guarantee that documents are up-to-date, precise, and version-controlled.

β€’ Assist in the preparation, distribution, and shipping of clinical trial documentation, including Investigator Site Files.

β€’ Administer project documentation and ensure the timely submission of records to the Trial Master File.

β€’ Track and maintain essential project information, including logs of medical questions and answers from sites.

β€’ Compile and disseminate meeting minutes for both sponsor and internal project meetings.

β€’ Keep accurate records of participating sites and study personnel.

β€’ Organize and supervise the completion of project-specific training within study teams.

β€’ Provide administrative and project tracking assistance to ensure the timely execution of project activities.

β€’ Collaborate with Project Managers, Clinical Research Associates, and other study team members to facilitate project delivery across various clinical trials.


⛳️ Requirements

β€’ A degree-level qualification or equivalent professional experience.

β€’ A minimum of one year of experience in a related position.

β€’ Proficient in English, with strong written and verbal communication capabilities.

β€’ Excellent interpersonal skills, with the ability to collaborate effectively across teams.

β€’ Capacity to work independently while also contributing as an active team member.

β€’ Demonstrated ability to manage multiple priorities and make sound judgments in a fast-paced environment.

β€’ Strong attention to detail with a commitment to quality and precision.

β€’ Outstanding organizational and problem-solving abilities.

β€’ Proficient in Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.

β€’ Familiarity with ICH, GCP, and relevant FDA or EU regulations.


🏝️ Benefits

β€’ Competitive benefits package based on location.

β€’ An inclusive and equitable workplace.

β€’ Equal employment opportunities.

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