Job Description

Summary
The Clinical Research Project Manager (Research Program Integrator - RPI) is responsible for leading and managing defined research activities for the Advanced Visualization Solutions (AVS) business within GE HealthCare. This role oversees cross-functional planning, execution, and communication to ensure timely, high-quality, and compliant delivery of research projects. The RPI manages the full lifecycle of research initiatives-from strategic planning through execution and closure-while meeting all quality, content, schedule, and budget targets.

Roles and Responsibilities
Project Execution

• Manage internal and external research activities, including GEHC- and Investigator-Sponsored Studies, product evaluations, reader studies, and other strategic research initiatives.
• Lead cross-functional teams to execute research projects in alignment with business needs and study plans.
• Partner with the Research Manager (RM) to prioritize and adjust study details as needed.

Compliance & Documentation

• Ensure all research activities comply with cross-functional standards, Phased Review Discipline, QMS, SOPs, GCP, and applicable regional regulatory requirements.
• Develop and manage essential research documents, including protocols, study plans, informed consent forms, and document storage.
• Maintain accurate and timely study records in systems such as Clinical Trials Management System, MyWorkshop, ClinicalTrials.gov, Support Central, and others.

Stakeholder & Site Management

• Negotiate budgets and contracts with external partners and manage payment processes.
• Conduct or coordinate training, site initiation, monitoring, and study closure activities.
• Serve as a quality control reviewer for peer studies, supporting review and approval of study activities.
• Build and maintain professional, productive relationships with external research partners and study sites.

Required Qualifications

• Bachelor's degree in life sciences, engineering, clinical field, or equivalent.
• Demonstrated progressive experience in project management of clinical or technical research in a clinical setting, industry, government agency, or a similar role in a medical device or pharmaceutical company.
• Strong understanding of Good Clinical Practices (GCP) and global/regional research or device regulations.
• Proven ability to build and sustain cross-functional relationships.

Desired Characteristics

• Master's degree in a scientific or related field, or an advanced medical degree.
• Professional certification in project management (e.g., PMP) or clinical research (e.g., CCRP, CCRA, CCRN).

Additional Information

GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

Relocation Assistance Provided: No

Job Tags

Relocation package,

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