Top Tech Jobs & Startup Jobs in Chicago, IL

The GCP Quality Governance Operations Lead oversees quality governance forums, directs assessments, coordinates reviews, and ensures compliance with GCP regulatory requirements while fostering effective communication across teams.

Support Marketing and Sales to generate campaigns and leads, analyze opportunities, schedule introductory business development calls, respond to inbound web leads, track prospect/client activity in CRM, and collaborate with sales leaders to develop market strategies across Parexel service lines.

The Business Operations Analyst supports Clinical Operations with contract management, financial planning, data analysis, and facilitates cross-department collaboration, ensuring documentation accuracy and efficiency improvements.

Lead end-to-end labeling process management including deviation/CAPA investigations, process governance, systems stewardship (Veeva RIMS, TrackWise, QDocs, Documentum), audit and inspection readiness, and cross-functional process improvements. Develop training and support regulatory intelligence, ensuring compliant labeling operations, KPI oversight, and coordination with Regulatory, Pharmacovigilance, Quality, and Manufacturing.

Lead design and reporting of end-to-end labeling KPIs and dashboards, ensure data integrity and governance, support compliance forums, audits, and digital enablement, and provide analytic insights to drive process improvements and CAPAs while offering cross-trained operational backup.

The Sr. Contracts Specialist amends, negotiates, and finalizes project budgets and contractual documents, ensuring quality deliverables and client interactions for Parexel's projects.

Lead GCP quality governance operations, manage quality metrics, ensure compliance across teams, and facilitate communication to support effective governance processes.

Design, build, and validate pipelines to ingest, standardize, and publish real-world healthcare datasets (claims, EMR, registry). Perform SQL, Python, and SAS transformations, OMOP conversions, QA, and vendor communications to deliver high-quality datasets for analytics and research.

As a Senior/Principal Regulatory Compliance Consultant, you will lead client engagements in QC Microbiology and sterile drug manufacturing, ensuring compliance and quality improvements while traveling extensively to support clients.

The Clinical Laboratory Study Manager manages clinical trial sample operations, ensures compliance, oversees data management, and liaises with various stakeholders to support biomarker evaluation.