Top Tech Jobs & Startup Jobs in Boston, MA

The SME will collaborate with engineers and data modelers to develop ontologies for pharmaceutical R&D, ensuring alignment with scientific workflows.

The Principal R Programmer develops custom programming code using R for clinical trial data analysis, ensuring compliance with CDISC standards, and performs quality control checks while training fellow programmers.

The Billing Specialist manages project and contract billing, maintains accounting records, oversees accounts receivable, and provides project reports, requiring strong accounting skills.

The Project Administrator supports the Regulatory Sciences Consulting team by reviewing client work products, managing submissions, and coordinating project logistics, ensuring deadlines are met.

Manage site identification, feasibility, and activation in clinical research projects while ensuring compliance. Analyze data for efficiency and assist in regulatory approvals.

The Central Study Coordinator manages remote site activities for projects, ensuring compliance, communication, and coordination. Responsibilities include data entry, subject re-consenting, and supporting study activities.

The Director of Business Development will sell Pharmacovigilance solutions, develop client relationships, negotiate contracts, and collaborate with marketing to drive sales growth.