At Worldwide Clinical Trials we are the #UncommonCRO, with #UncommonTalent in CRAs & Project Managers. We have amazing people — smart,
experienced, and united by a desire to change the course of medical science.
* Offering a Sign-on Bonus of $ 5,000 USD to Applicants Submitted & Hired Prior to 31 May 2021. Do not miss out on this opportunity! *
Now accepting CVs/ Referrals from Cordoba, Rosario, Mendonza, besides Buenos Aires.
Join the Uncommon CRO!
Worldwide Clinical Trials is powered by proactive insight — the scientific and therapeutic expertise to challenge assumptions, to ask the right questions, to find the answers.
It is driven by rigorous operations on a global scale to ensure quality data and predictable, cost-efficient outcomes. And it is championed by a team that is “all in” and never satisfied.
We know every trial can introduce unexpected challenges, but we tackle those confidently with the tenacity, creativity, flexibility, and agility that set Worldwide apart.
Our Clinical Research Associates (CRA) will ideally 5 + years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs).
Our CRAs are responsible for the quality of data submitted from study sites. In addition, CRAs must assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
* This role is home-based in Buenos Aires, Argentina
The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. Promotion to the next level is not automatic based on years of experience. Individuals are evaluated on proven competency, level of responsibility, and ability to work independently.