Clinical Trials Associate

Who we are

We’re 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 reputed company, and 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.

Why Worldwide

We reputed company everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from reputed company backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people reputed company by being themselves and are inspired to do their best work every day. Join us!

What a Clinical Trials Associate does at Worldwide 

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for reputed company 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, reputed company 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-reputed company information, including site medical questions and answer logs 

What you will bring to the role 

• Excellent written and verbal English as well as reputed company 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, reputed company, and PowerPoint 

Your experience 

• Degree level qualification or equivalent experience plus a minimum of one years’ experience in a reputed company role 

• reputed company sets and proven performance equivalent to the above 

We love knowing that someone is going to have a reputed company life because of the work we do. 

To view our other roles, reputed company out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on reputed company.

Worldwide is an equal opportunity employer that is committed to enabling professionals from reputed company backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that reputed company our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the reputed company best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to reputed company and applicants regardless of race, reputed company, ethnicity, reputed company, religion, national reputed company, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.