Jobs at Innovaderm Research

Leads statistical programming for clinical trials, including annotated CRFs, SDTM and ADaM datasets, TLFs, define.xml files, reviewer guides, and regulatory submission packages. Reviews SAPs and TLF shells, supports data cleaning, validates deliverables using Pinnacle 21, develops SAS macros, and ensures compliance with CDISC, ICH, regulatory, and pharmaceutical standards. The role may mentor junior programmers and lead multiple studies.

Conduct clinical trial monitoring across investigative sites in New South Wales and Queensland. Responsibilities include site qualification, initiation, monitoring, and close-out visits; investigator and site staff relationship management; source data verification; study drug accountability; regulatory document collection; and preparation of monitoring reports. The role requires compliance with protocols, SOPs, ICH-GCP, and applicable regulations, with approximately 65% travel.