Clinical Trials Associate- US/Canada
Worldwide Clinical Trials•Carolina, NC
About The Position
The Clinical Trials Associate provides administrative and project-tracking support to clinical project teams, ensuring tasks across assigned projects with Project Delivery services are completed accurately and on time. The role supports project access, document quality and version control, clinical trial document preparation and shipment, trial master file submissions, and tracking project-related information.
Requirements
- Degree-level qualification or equivalent experience.
- At least one year of experience in a related role.
- Excellent written and verbal English, and fluency in the language of the country of location.
- Ability to handle multiple tasks and exercise independent judgment.
- Strong attention to detail and focus on quality of work.
- Strong organizational and problem-solving skills.
- Excellent skills in MS Office applications, including Outlook, Word, Excel, and PowerPoint.
- Skill sets and proven performance equivalent to the stated qualifications.
Responsibilities
- Arrange and track system access for project team members, including Project Managers, Lead CRAs, and CRAs.
- Maintain and quality-audit project portals to ensure they contain the most recent document revisions.
- Assist the project team with preparing and shipping clinical trial documentation, including Investigator Site Files.
- Maintain version and quality control of project documentation and submit documents to the trial master file.
- Assist with tracking and maintaining project-related information, including the site medical question and answer log.
Benefits
- Competitive benefits package, depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
