[Hiring] Clinical Trials Associate @Worldwide Clinical Trials

Role Description

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What you will do

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
• Maintain and quality audit to ensure the most recent revisions of documents are on the project portals
• Assist the project team with the preparation and shipment of clinical trial documentation, including the Investigator Site File
• Maintain version and quality control of project documentation and submit to the trial master file
• Assist with the tracking and maintenance of project-related information, including site medical questions and answer logs

Qualifications

• Excellent written and verbal English as well as fluency of the language of the country of location
• Ability to handle multiple tasks and exercise independent judgment
• Strong attention to detail and focus on the quality of work
• Strong organizational and problem-solving skills
• Excellent skills in MS Office applications, including Outlook, Word, Excel, and PowerPoint

Requirements

• Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
• Skill sets and proven performance equivalent to the above

Benefits

• Equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law