
Clinical Trials Coordinator
Há 9 horas
We are seeking a highly organized and detail-oriented Clinical Trials Associate to provide administrative and project tracking support to our clinical project team. This role is ideal for someone who enjoys working on multiple tasks, exercising independent judgment, and ensuring timely completion of projects.
Main Responsibilities:
- Arrange and track system access for project team members, ensuring they have the necessary permissions and credentials to perform their tasks.
- Maintain and quality audit documents to ensure the most recent revisions are available on project portals.
- Assist with the preparation and shipment of clinical trial documentation, including Investigator Site Files.
- Maintain version and quality control of project documentation, submitting it to the trial master file.
- Track and maintain project-related information, including site medical questions and answer logs.
Requirements:
- Excellent written and verbal English skills, as well as fluency in Spanish.
- Ability to handle multiple tasks and exercise independent judgment.
- Strong attention to detail and focus on quality work.
- Strong organizational and problem-solving skills.
- Proficiency in MS Office applications, including Outlook, Word, Excel, and PowerPoint.
Experience:
- Degree level qualification or equivalent experience plus a minimum of one year's experience in a related role.
- Skill sets and proven performance equivalent to the above.
This is an excellent opportunity for someone looking to grow their career in clinical trials administration. If you have the required skills and experience, we encourage you to apply for this role.
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