Roles and Responsibilities
- Work with product leaders across MIM franchises to identify research needs, estimate resources, and establish study plans aligned to product and clinical priorities.
- Manage GEHC‑sponsored and investigator‑initiated studies from planning through completion, ensuring timelines, deliverables, and quality expectations are met.
- Lead reader studies, evaluations, and other research activities that inform product development and clinical validation.
- Coordinate development and review of study budgets; manage and generate contracts with Legal support; process milestone‑based payments and ensure financial accuracy.
- Maintain audit‑ready documentation in compliance with GEHC SOPs and research governance requirements.
- Track study status, risks, and deliverables; prepare reports and lead operational reviews with stakeholders.
- Build strong working relationships with research sites, serving as the main operational contact.
- Support sites through clear communication, timely issue resolution, and high‑quality study coordination.
- Contribute to improvements in workflows, templates, documentation standards, and operational systems.
- Collaborate closely with regional research managers, engineering, QA/RA, Medical, service teams, finance, and modality partners to ensure successful and efficient delivery of research outcomes.
Required Qualifications
- Bachelor's degree from an accredited university or college
- 2+ years of project management in a clinical or industry research setting
- Strong communication and interpersonal skills
- Demonstrated success managing detailed documentation and multi‑party coordination
- Ability to balance multiple projects in a fast‑paced environment
- Strong organizational and problem‑solving skills with a solutions‑oriented mindset
- Experience working on cross‑functional teams
- Proven ability to build effective and lasting professional relationships
Desired Characteristics
- Experience with MIM software tools or familiarity with clinical applications
- Project management or clinical research certification (PMP, CCRP, CCRA, CCRN)
- Strong attention to detail and ability to work independently
- Experience with global or virtual teams
- Background in medical imaging environments
- Familiarity with GE HealthCare tools and processes (e.g., SC, SSP, AST)
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
Top Skills
What We Do
Every day millions of people feel the impact of our intelligent devices, advanced analytics and artificial intelligence.
As a leading global medical technology and digital solutions innovator, GE Healthcare enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by its Edison intelligence platform.
With over 100 years of healthcare industry experience and around 50,000 employees globally, the company operates at the center of an ecosystem working toward precision health, digitizing healthcare, helping drive productivity and improve outcomes for patients, providers, health systems and researchers around the world.
We embrace a culture of respect, transparency, integrity and diversity.
