CDM - RAVE EDC EXPERTISE @ IQVIA
Join our dynamic clinical research team as a Clinical Data Manager (CDM) with specialized expertise in Rave EDC. In this remote-based role, you will lead end-to-end data management activities, ensuring the integrity and accuracy of clinical trial data from inception through to the final database lock. We are looking for dedicated professionals who thrive in a fast-paced environment and are committed to maintaining the highest standards of data quality in the life sciences industry. Your primary responsibilities will include overseeing Clinical Data Management vendors, reviewing clinical protocols, and designing Case Report Forms (CRFs) to support study objectives. You will manage the entire data lifecycle, ensuring all tasks are performed in accordance with organizational Standard Operating Procedures (SOPs). To be successful, you must have an immediate or short notice period (30 days maximum) and significant hands-on experience with Rave EDC; please note that candidates with only eTMF experience will not be considered.
Key Requirements
Expertise in Rave EDC
End-to-end CDM project management
Vendor setup and oversight
Responsibility for data review
Responsibility for data delivery
Protocol review proficiency
CRF design expertise
Execution of database lock procedures
Adherence to Standard Operating Procedures (SOPs)
Availability within a 30-day notice period