Clinical Trials Associate
4 semanas atrás
BRL 163.000 - 219.000
Clinical Trials Associate - Argentina- RemoteJoin to apply for the Clinical Trials Associate - Argentina- Remote role at Worldwide Clinical Trials .
OverviewWe’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. 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 WorldwideWe 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 WorldwideAs 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 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 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
- Excellent written and verbal English as well as fluency 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, Excel, and PowerPoint
- 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
- Seniority level: Entry level
- Employment type: Full-time
- Job function: Research, Analyst, and Information Technology
- Industries: Research Services
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, 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.
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