Senior Clinical Trials Associate

Worldwide Clinical Trials; Buenos Aires; Presencial; ARS 52.819.000 - 83.001.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials seeks a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects are performed timely and accurately.

The role requires excellent written and verbal English as well as fluency in the language of the country of location, strong interpersonal and organizational skills, and attention to detail with a minimum of two years’ related experience.

Formación

• Degree or equivalent qualification with at least two years’ experience.
• Excellent written and verbal English; fluency in the country language.
• Strong interpersonal, organizational and problem-solving skills.
• Attention to detail and commitment to quality work.

Responsabilidades

• Arrange and track system access for project team.
• Maintain and quality audit project documents on portals.
• Assist with preparation and shipment of clinical trial documentation.
• Maintain version control of project documentation and submit to trial master file.
• Assist tracking of site medical question and answer log.
• Generate and distribute minutes for sponsor and internal meetings.

Conocimientos

English proficiency

Interpersonal skills

Attention to detail

Organizational skills

Problem-solving skills

Educación

Bachelor's degree or equivalent

Descripción del empleo

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.

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.