Top Tech Jobs & Startup Jobs in Boston, MA

Accountable for coordinating activities for site activations and maintenance, ensuring compliance with regulations and processes. Acts as a liaison, resolves issues, and supports project outcomes in clinical studies.

The Manager, Production Operations oversees day-to-day production activities, ensuring efficiency, quality standards, and alignment with organizational goals while leading a team and collaborating across departments for process optimization.

The Clinical Study Specialist coordinates clinical trials by managing data, scheduling meetings, conducting document reviews, monitoring trials, and engaging with clinical trial sites.

The Clinical Study Specialist organizes reports, schedules meetings, manages study documents, tracks trial progress, and communicates with sites for clinical trials.

Negotiate, draft, review, and finalize clinical trial agreements, amendments, and ancillary documents with study sites. Maintain stakeholder communication, track contract progress in ICON/client systems, identify risks, support site start-up, file contractual documents, and participate in study team calls while adhering to SOPs and training requirements.

This role involves overseeing clinical trials for cardiovascular/electrophysiology medical devices, ensuring regulatory compliance, and managing site relationships.

The Clinical Research Associate II conducts site visits for clinical trials, ensures compliance, collaborates with sites, and maintains data integrity.

As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.