Clinical Project Manager

Terumo Medical Corporation

Clinical Project Manager managing clinical trials from planning to final report at Terumo Medical Corporation. Collaborating on study budgets, site management, and regulatory compliance.

Posted 6/6/2026full-timeSomerset • New Jersey • 🇺🇸 United StatesMid-LevelSenior💰 $105,400 - $144,870 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the development of project related deliverables including the project management plan, overall clinical budget, study timeline, risk management / contingency plan, monitoring plan, communication plan, etc.
Responsible to develop of study related documents, including protocol, informed consent, IB, regulatory binder, training materials, etc. and provide input to case report forms.
Responsible to manage and track the overall study budget, track and administer payments, and provide financial updates.
Responsible for the proactive management and conduct of clinical trials.
Provide centralized site support, communication and coordination to assure timely completion of start-up, enrollment and all other study activities.
Assist in the review site visit reports and enrollment progress and monitors the study for protocol, federal, and local compliance.
Support vendor selection process, including RFP to contract and change order process for CROs and other external service providers (ESP).
Provide day to day management of ESPs ensuring quality deliverables and adherence to the scope of work;
Manage clinical supply shipments and inventory.
Ensure compliance with Terumo policy, procedures and SOPs, GCP, and local, regional and federal regulations.
Provide periodic updates, reports, etc. as requested.
Manage ongoing communication of operation issues and provides progress reports to the study team.
Assist with Database freeze, Database lock, annual progress reports, and final clinical study reports.
Responsible for Site Management and Monitoring as required.

Requirements

What you’ll need

Bachelors degree in a clinical or scientific discipline
minimum of 5 years clinical research experience; or equivalent combination of education, training and work experience
at least 2 years of clinical trial / clinical research site management, monitoring and project management / lead experience
Medical device industry experience strongly preferred
Direct experience with site and / or sponsor level audits or FDA BIMO investigation(s) preferred

Benefits

Comp & perks

annual bonus
paid vacation
paid holidays
health, dental and vision benefits
401(k), with matching contributions
tax advantage savings accounts
legal plan
voluntary life and AD&D insurance
voluntary long-term disability
short term disability
critical illness and accident insurance
parental leave
personal leave
tuition reimbursement
travel assistance
employee assistance program

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical researchproject managementbudget managementrisk managementprotocol developmentregulatory compliancesite managementmonitoringvendor managementdata management

Soft Skills

communicationcoordinationproblem-solvingleadershiporganizational skillsattention to detailproactive managementteam collaborationreportingtime management

Certifications

Bachelor's degree in clinical or scientific disciplineclinical research certificationproject management certification