Global Clinical Trial Program Manager

Terumo Cardiovascular Group; New Jersey; On-site; USD 105,000 - 145,000; Full time

Benefits offered by this job

Annual bonus

Paid vacation

401(k) with matching contributions

Health, dental and vision benefits

Job summary

Terumo Medical Corporation in the United States seeks a Clinical Project Manager (CPM) to oversee trials from planning to final report. You will help develop trial strategy, timelines, budgets, risk plans, site selection and monitoring, data management coordination, and vendor management to ensure on-time delivery and quality.

You will produce study documents, manage budgets, monitor enrollment, support regulatory compliance, and coordinate with CROs and ESPs.

Qualifications

• Clinical project management experience in medical device trials
• Budgeting and financial tracking in clinical studies
• Regulatory compliance and GCP knowledge
• Site management and monitoring experience

Responsibilities

• Develop clinical trial strategy, timelines and budgets.
• Manage overall study budget, payments and financial updates.
• Coordinate site selection, monitoring, and CRO/vendor management.
• Ensure regulatory compliance and data management coordination.
• Support site visits, enrollment tracking and study reports.
• Travel as required to trial sites and audits.

Job description

Terumo Medical Corporation in the United States seeks a Clinical Project Manager (CPM) to oversee trials from planning to final report. You will help develop trial strategy, timelines, budgets, risk plans, site selection and monitoring, data management coordination, and vendor management to ensure on-time delivery and quality.

You will produce study documents, manage budgets, monitor enrollment, support regulatory compliance, and coordinate with CROs and ESPs.