other
Posted 3 weeks agoAdministrative Coordinator
at Fortrea
On-site
Responsibilities
- Support us on our mission “To help make life-changing healthcare solutions possible”.
- Determine the panel of eligible and standby subjects for specific studies after receiving completed data from the physicians Conduct daily QC of screening Case Report Forms (CRF).
- Maintain exquisite documentation and accurate record keeping of the process: from organizing, overseeing and compiling CRF workbooks, managing subject ID codes and other info to CRFs or ICFs, to maintenance of the post screening data archiving process relating to screening data, tests and measurement results.
- Ensure that the highest levels of ethical and medical confidentiality are maintained and that volunteer’s records are stored securely with restricted access.
Requirements
- Experience in clinical trials, lab, hospital or similar setting would be an advantage, but not essential.
- Able to demonstrate working knowledge of Microsoft Office (Outlook, Word, Excel) ON A NORMAL DAY… You will support our Clinical Operations team in their participant recruitment efforts, ensuring the correct eligibility of participants in the right clinical trial.
Experience
- WHO YOU ARE Typically 3+ years’ administrative experience.
Additional details
- What if your administrative support expertise could help us accelerate that journey? FORTREA IN LEEDS – WHERE MEDICAL BREAKTHROUGHS BEGIN At Fortrea, our world-class Clinical Research Unit in Leeds sits at the heart of innovation.
- Just a short 7-minute walk from the train station, this 65,000 ft², 100-bed facility is a cornerstone of our global operations.
- Dedicated to Early Clinical Research, it’s where life-saving medicines begin their journey .
- And this is where you come in because we are expanding and now seeking our new Clinical Trial Participant Recruitment Administrative Coordinator.