ICON Strategic Solutions

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patie More...

Doing the production and QC programming of SDTM datasets, analysis datasets (ADaM), tables, listings, and figures, for multiple clinical trials using SAS software. Integration data across multiple studies or drug programs. Working with minimal supervision under the direction of a More...

. Maintaining and motivating a successful team by recruiting, training, and coaching employees; ensuring a safe, secure, and compliant work environment; providing your team with professional development and growth opportunities. . Within your own statistical programmer team, monitori More...

Create, validate, execute and generate statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures) . Create and finalise project or departmental level macros . Create and finalise programming specifications/mock-ups . In accordanc More...

Provide input in protocol development/amendment Review data to ensure concordance across efficacy assessments Perform BILAG and MDAAT grading for each organ system, if applicable. Trains study teams (protocol specific training on efficacy tools). Start-up activities including si More...

Serve on Sponsor Standards and Technology Leadership teams. Consult with clients on sponsor-specific CDISC centric implementation projects. Participate in industry groups focused on the development of standards related initiatives (e.g. CDISC, PhUSE etc.). Author, maintain, imple More...

Accountable for delivery of global trials within agreed/projected life of trial budget. Ensures accurate trial budget management, updates for scope changes and reconciliation of assigned trials for both Out of Pocket costs and FTE costs Lead the cross-functional Trial Team; Trackin More...

. Maintaining and motivating a successful team by recruiting, training, and coaching employees; ensuring a safe, secure, and compliant work environment; providing your team with professional development and growth opportunities. . Within your own statistical programmer team, monitori More...

. Create, validate, execute and generate statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures) . Create and finalise project or departmental level macros . Create and finalise programming specifications/mock-ups . In accordanc More...

A minimum of 6 years relevant experience of successfully performing the role of Statistical Programmer, preferably in the clinical research industry Good understanding of global clinical trial practices, procedures, methodologies and regulatory Good knowledge with PK/PD data Requ More...

Ensure regional/global clinical operations deliverables progress according to agreed upon timelines and milestones as leader of the Study Management Team. This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor setu More...