Are you an experienced Project Coordinator, ideally with Clinical experience? Are you looking for your next challenge within a growing team? The eCOA business unit are looking for enthusiastic individuals with an eye for detail and the ability to work in an organised manner in a fast paced environment.
ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that our customers can move ahead with confidence. With more than 45 years of clinical and therapeutic experience, ERT balances knowledge of what works with a vision for what’s next, so it can adapt without compromising standards.
Powered by the company’s EXPERT® technology platform, ERT’s solutions enhance trial oversight, enable site optimization, increase patient engagement, and measure the efficacy of new clinical treatments while ensuring patient safety. Over the past four years, more than half of all FDA drug approvals came from ERT-supported studies. Pharma companies, Biotechs, and CROs have relied on ERT solutions in 9,500+ studies spanning three million patients to date. By identifying trial risks before they become problems, ERT enables customers to bring clinical treatments to patients quickly – and with confidence. For more information, go to ert.com or follow us on LinkedIn, Twitter, and Facebook.
Responsible for assisting Project Management personnel with various tasks throughout the study lifecycle the essential duties and responsibilities include:
a. Database setup
b. Study documentation development
c. Equipment distribution/tracking
d. Report creation/distribution
e. Archival of study documentation
a. Assistance with documentation/database updates due to scope changes
b. Follow-up related to invoice reconciliations
c. Preparation of reports in support of study forecasting activities
Other Duties and Responsibilities: