"Join Us as a Principal Programmer Analystt – Make an Impact at the Forefront of
Innovation
We have successfully supported the top 50 pharmaceutical companies and more than
750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5
years.
As part of our expert team, you’ll have the prospect to ensure operational
excellence that makes a real difference in clinical trials. As a Principal
Programmer Analyst, you will act as the lead programmer, project lead, or
project oversight lead on multiple projects, overseeing the statistical and
bioinformatics programming aspects of clinical trials from design through
analysis and reporting. You will organize teams and implement study strategies
to ensure process and programming efficiencies, and the creation and maintenance
of programs for statistical report generation and program validation. You will
represent the department within the company and in interactions with client
companies and regulatory agencies.
Additionally, you will provide training,
guidance, and project leadership to junior team members.
What You’ll Do:
Experience on SDTM, ADAM and TLF is mandatory
• Serves as a lead programmer or project lead on studies or drug programs of all
complexities and size scales. Works directly with project team leaders and
client representatives to conduct team meetings, develop and maintain project
timelines, assess and forecast resources, and ensure adherence to study budgets
and any relevant contractual obligations or limits with clients.
• Suggests, plans and provides developments to tools and techniques for
improving process efficiencies. Actively contributes to process or tool
improvement efforts including leadership of solution teams. Represents the
department to clients on study matters, bid defenses or submission or review of
clinical data to regulatory authorities, directly contributing to proposals and