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The Technical Project Manager will support project management through planning, coordinating, and monitoring technology solutions for various functional teams, using methods established by the TPM group.

As a Specialist in Regulatory Operations, oversee compliance and regulatory activities for clinical trials, particularly for U.S. sites, ensuring adherence to FDA and global standards. Support IRB submissions and maintain essential regulatory documentation.

The Specialist coordinates user access and management for clinical systems, monitors compliance, supports onboarding/offboarding, and collaborates with stakeholders to ensure study readiness and system functionality.

The Specialist, Regulatory Operations oversees regulatory activities for clinical trials, ensuring compliance and supporting site operations. Responsibilities include managing IRB submissions, regulatory documentation, and collaborating with cross-functional teams.

Manage Site Support Solutions team, oversee daily operations, hire and train staff, ensure performance metrics are met, and collaborate with leadership and sponsors.

The Senior HR Business Partner will align business strategy with people plans, oversee talent management, ensure compliance in HR practices, and mentor junior HR staff.

The Senior Software Engineer will develop full-stack applications using TypeScript, collaborate with designers, implement APIs, and ensure code quality in a remote setting.

The Senior Data Engineer will design, develop, and maintain data pipelines, optimize data performance, and collaborate with stakeholders to deliver effective data solutions.

The Senior Enterprise Performance Analyst will enhance organizational performance by developing dashboards, analyzing key performance data, and mentoring junior analysts.

The Principal Investigator oversees clinical trials, ensuring protocol adherence and patient safety while managing study staff and participating in regulatory compliance activities.