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Worldwide

Senior Clinical Trials Associate

Buenos Aires, Argentina · Virtual Mexico

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hirly's read of this role

Seniority
Senior
Countries
AR, MX
Work mode
On-site / unstated
First seen by hirly
18 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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 the Senior Clinical Trials does

The Senior Clinical Trials Associate is 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 assure the most recent revisions of documents are on project portals

Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File

Maintain version and quality control of project documentation and submit to trial master file

Assist with the tracking and maintenance of project related information, including site medical question and answer log

Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management

What you will bring to the role

Excellent written and verbal English as well as fluency of the language of the country of location

Strong interpersonal skills

Strong attention to detail and focus on quality of work

Strong organizational and problem-solving skills

Your experience

Degree level qualification or equivalent experience plus a minimum of two years’ 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 .

Original posting on Worldwide's site ↗

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