- Location
- Virtual Argentina
- Workplace
- Remote
- Type
- Full-time
- Department
- Healthcare
- Seniority
- Entry
- Source
- Workday
Description
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 Worldwide Clinical Trials, 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 believe 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 all 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 thrive 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 all assigned projects with Project Delivery services are performed in a timely and accurate manner.
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.
What you will bring to the role
Excellent written and verbal English as well as 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 the quality of work
Strong organizational and problem-solving skills
Excellent skills in MS Office applications, including Outlook, Word, Excel, and PowerPoint
Your 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
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check 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 LinkedIn.
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. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very 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 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.
