* Leads and works collaboratively with multiple
functions including but not limited to Biostatistics, Statistical
Programming, Clinical Data Management, Clinical Science, Drug Safety,
Medical Writing, Regulatory, Project Management, Research, and IT to
develop internal standards, tools/systems, and processes for data
collection, statistical data analysis and reporting. * Identifies,
develops, and implements new standards, tools/systems, and/or new
processes to increase MaxisIT productivity and efficiencies.
*
Ensures adequate development and implementation of SOPs and Working
Instructions within MaxisIT and adequate integration of MaxisIT
functions (CDM, Statistical Programming, and Biostatistics).
* Manages direct reports (up to 5) and/or teams of data managers/ statistical programmers, and/or statisticians.
* Evaluates ongoing processes and identifies gaps for process improvements.
* Coordinates and provides solutions for special requests from other functions.
* Plans, negotiates/recruits, and manages external partnerships,
alliances, collaborators, contractors, CROs, and FSPs for MaxisIT as
necessary.
Salary:
As per Industry Standards
Industry:
Pharma / Biotech / Clinical Research
Functional Area:
IT Software - Application Programming, Maintenance
Role Category:
Programming & Design
Role:
Project Lead
