Pharma Medica Research (PMRI) Inc. is a Contract Research Organization committed to innovation and the delivery of high‑quality research. We are currently looking for a CDM Data Coordinator to join our team.

Duties and Responsibilities

• Perform User Acceptance Testing (UAT) of the study electronic Case Report Forms (eCRFs) from a data entry perspective to ensure the functionality of programmed edit checks and the overall usability of the eCRFs.
• Accurately enter required data from clinic source documents into the EDC system and/or validated Excel spreadsheets, meeting study timelines, SOPs, GCDMP, and DEGs while maintaining an acceptable query rate.
• Code medical history, concomitant medications, and adverse events in the EDC system using MedDRA and the WHO Drug Global B3 Dictionary.
• Respond to data queries promptly.
• Manage laboratory data by compiling and tracking requisitions, requesting electronic transfers, importing data ...