Responsible for analyzing scientific and operational data to support the Data Surveillance process
Develops Data Surveillance Plans (DSPs) and conducts defined project reviews
Attends internal and external Data Surveillance meetings, presenting relevant findings to the project team
Reviews relevant data to support reviews designated for the DS Analyst per the project specific Data Surveillance Plan
Document findings from Data Surveillance activities in the DS Findings Form and other appropriate systems
Requirements
2 or more years of relevant medical, clinical or data management work experience recommended
Experience of working within an adaptive monitoring design study and/or participating in a Central Monitoring/Data Surveillance process highly recommended
Basic SAS programming and/or SQL script writing required
Educated to a degree level (medical, biological science, pharmacy and/or data analytics, preferred) or relevant clinical, technology or business equivalent