Our client, a Hertfordshire based Pharmaceutical company, is currently seeking an experienced Study Data Manager to join their team on a permanent basis due to a period of growth.
Within this role you will be responsible for the following:
-Carry the paper CRF design and eCRF accordance with the study protocol
-Coordinate activities with ADM
-Perform data extraction for provision statisticians
-Write the Data-Management plan and program / validate the consistency tests in Capture system and SAS
-Review generated queries before sending investigators.
-Ensure reconciliation of SAEs and medical coding
-BAC +4/5 with specialization in Data Management and Statistics
-At least 2/3 years experience in the management of clinical data
-Programming experience with the necessary SAS
-Good knowledge of EDC and especially the Capture tool system, especially the Designer modules, Export, Test, Coder
-Good knowledge of coding dictionaries (MedDRA and WhoDrug)
-Knowledge of CDISC is a plus
For further details about this role or other opportunities within Data Management please contact Tim Barratt on or email a copy of your CV to firstname.lastname@example.org