EDC Clinical Trial Designer - FSP (Homebased - UK)

Minimum of 2 years of Clinical Data Management experience using electronic data capture systems.

Familiarity with clinical research processes and CDISC/CDASH/SDTM standards

Strong attention to detail and a commitment to high quality work, customer service and getting things right the first time with minimal errors.

Experience in the planning and management of clinical trials in the biopharmaceutical industry or a related field

Proficiency with the following in Central Designer/Studio

Understanding detailed data collection requirements based on the protocol and input from study team members.

Validation of study design for forms and schedule design.

Test steps development and QC of forms.

Basic understanding of activities needed for data integrations, local lab management, coding functionality.

Input into design of post-production form changes to the live trials.