Top Tech Jobs & Startup Jobs in Chicago, IL

ProPharma seeks an auditor for a GDP project in Brazil lasting 2 days, requiring expertise in regulatory compliance and Portuguese language skills.

Conduct a PMDA audit and gap assessment for a New Jersey facility toensure compliance with Japanese GMP standards, including a report and training presentation.

Support remote site activities for assigned clinical research projects, including site communications, document submissions, pre-screening support, data entry, query resolution, database monitoring, IRB/FDA-compliant documentation, study closeout assistance, and other site-related tasks as directed.

Monitor and triage pharmacovigilance inboxes, perform case book-in and duplicate searches, redact PHI, facilitate literature activities, triage regulatory database searches, prepare draft reports, and enter basic (and, with training, full) case data into the safety database.

Responsible for coordinating and supporting remote site activities for clinical research projects, including recruitment, documentation, and communication with study sites.

The Compliance Consultant will conduct a GDP Gap Assessment for biotech, med device, and pharmaceutical organizations, focusing on distribution regulations in Brazil.

Manage business development for Clinical Research Solutions, building client relationships, generating leads, negotiating contracts, and collaborating with internal teams for strategic sales initiatives.

The Senior Director of PV Client Support manages client services, oversees team operations, sets strategic goals, and ensures compliance while fostering team development.

The Senior Director of PV Client Support leads and manages teams in pharmacovigilance, driving operational goals, overseeing budgets, and ensuring compliance. They engage in client relationships, negotiations, and guide internal workflow improvements, all while monitoring efficiency and quality metrics in a fast-paced environment.

The Process Engineer will provide engineering guidance, review materials, draft documentation for FDA submission, and support device testing and qualifications.