Top Tech Jobs & Startup Jobs in Boston, MA

As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

As a Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations, and provide support to trials.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring protocol compliance, data integrity, and patient safety, while collaborating with site staff and preparing study documentation.

The Feasibility Principal Analyst leads feasibility strategy and analysis for clinical studies, synthesizing data to inform study planning and enrollment decisions while mentoring junior team members.

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

The manager will oversee operational planning, implement process improvements, manage KPIs, and coach team members to enhance efficiency.

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.