[Hiring] Clinical Trials Associate @Worldwide Clinical Trials

Role Description

As a Clinical Trial Associate, you’ll play a vital role in supporting the successful delivery of clinical trials by providing essential administrative and project coordination support to global project teams. Your work will help ensure critical study activities stay on track, documentation remains accurate, and project information is maintained to the highest quality standards.

Working closely with Project Managers, Clinical Research Associates, and other study team members, you’ll contribute to the smooth execution of clinical trial projects through effective coordination, organization, and attention to detail. Your ability to manage multiple priorities and maintain quality will have a direct impact on project success.

This is an opportunity to be a key partner to cross-functional teams, helping ensure that important clinical trial processes are completed accurately, efficiently, and in compliance with applicable requirements.

Qualifications

• Degree-level qualification or equivalent experience.
• Minimum of one year of experience in a related role.
• Proficiency in English, with excellent written and verbal communication skills.
• Strong interpersonal skills and the ability to collaborate effectively with cross-functional teams.
• Ability to work independently while also contributing as an effective team member.
• Strong organizational, problem-solving, and multitasking skills in a fast-paced environment.
• Excellent attention to detail and commitment to producing high-quality work.
• Advanced proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.
• Working knowledge and understanding of ICH, GCP, and applicable FDA or EU regulatory requirements.

Requirements

• Coordinate and track system access for project team members to support efficient study execution.
• Maintain project portals and perform quality checks to ensure documentation is current and accurate.
• Support the preparation, distribution, and shipment of clinical trial documentation, including Investigator Site Files.
• Manage document version control and submit project documentation to the Trial Master File.
• Track and maintain project-related information, including site medical question and answer logs.
• Prepare and distribute meeting minutes for sponsor, project, and internal management meetings.
• Maintain accurate records of participating sites and study personnel.
• Coordinate and track project-specific training assignments and completion across study teams.
• Contribute to additional project and administrative activities as needed to support project delivery.

Company Description

Worldwide is a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity.