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Recently posted jobs
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Research Associate II, you'll oversee clinical trials, ensure data integrity and patient safety, and collaborate with site staff.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Start Up Project Manager oversees global study start up activities, ensuring site activations and project timelines meet targets across clinical trials.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Study Start Up CRA is responsible for site selection, start up activities, ensuring compliance with relevant regulations, and collaborating with various stakeholders to meet study timelines.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Manager of Clinical Operations, you will oversee clinical trials, ensuring compliance with regulations, optimizing processes, and mentoring junior staff while maintaining stakeholder communications.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Clinical Research Associate, you will monitor Oncology studies, coordinate activities, ensure compliance, and maintain strong relationships with stakeholders to ensure patient safety and efficient study operations.
Healthtech • Biotech • Pharmaceutical • Manufacturing
Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Senior Issue Lead manages Major Quality Event investigations, coordinates audits, ensures compliance with GCP standards, and trains Issue Leads. This role involves root cause analysis, process improvement, and leading quality assessments.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Third Party Quality Lead manages third-party quality risks in clinical operations, ensures GCP compliance, and oversees vendor performance and quality systems.
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Quality ICM Issue Lead oversees quality event case management, leading investigations, notifications, root cause analysis, and process improvements within clinical development.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.
Healthtech • Biotech • Pharmaceutical • Manufacturing
As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.