Research Program Integrator

GE HealthCare

3d•$110,000 - $165,000

About The Position

The Research Program Integrator (RPI) manages clinical and technical research activities for assigned GE HealthCare businesses across multiple global regions. The role leads cross-functional planning, execution, and communication for internal and external studies, including GE-sponsored and investigator-sponsored research. The RPI oversees research projects throughout their lifecycle—from development and active management through closure—ensuring quality, content, schedule, and budget targets are met. The position coordinates research teams and partners, maintains study documentation and records, supports project budgets, contracts, payments, and vendors, and ensures compliance with applicable quality, clinical practice, and regulatory requirements. It also provides updates to stakeholders, supports portfolio prioritization, and contributes to process improvements and research project management practices.

Requirements

Bachelor’s degree in life sciences, engineering, clinical sciences, or a related field; equivalent combinations of education and experience may be considered.
At least 5 years of experience in clinical or technical research programs in a clinical setting, industry, government agency, or a similar role in a medical device or pharmaceutical company.
Experience with medical device, healthcare technology, pharmaceutical, or clinical research organizations.
Familiarity with investigator-sponsored and industry-sponsored research.
Knowledge of Good Clinical Practice (GCP), clinical research regulations, and research documentation requirements.
Demonstrated project management, analytical, and problem-solving skills.
Strong written and verbal communication skills.
Experience working effectively with cross-functional teams.
Ability to manage multiple projects simultaneously while maintaining attention to detail.

Nice To Haves

Experience with Clinical Trial Management Systems (CTMS) and regulatory reporting systems.
Experience managing research budgets, contracts, and external partners.
Understanding of product development and cross-functional project environments.
Experience with global teams.
Knowledge of GE HealthCare tools and processes, such as Support Central, SSP, AST, and MyWorkshop.
Ability to influence stakeholders, build consensus, and drive project execution.

Responsibilities

Lead assigned research projects from planning through completion, including timelines, budgets, risks, deliverables, and reporting.
Coordinate cross-functional teams across Research, Medical Affairs, Clinical Development, Engineering, Product Management, Quality, Regulatory, and Operations.
Ensure compliance with Quality Management System requirements, SOPs, Good Clinical Practice (GCP), and applicable regulatory requirements.
Develop and maintain study documentation, including protocols, plans, informed consent forms, reports, and project records.
Oversee study execution activities, including initiation, monitoring, training, enrollment progress, and closure with internal teams and external research partners.
Identify and resolve project risks, operational issues, and cross-functional challenges.
Support contract, budget, payment, and vendor management activities.
Maintain accurate records in approved systems, including CTMS and regulatory databases.
Provide project updates to stakeholders and support portfolio prioritization with Research Managers.
Contribute to process improvements and research project management best practices.

Benefits

Medical insurance
Dental insurance
Vision insurance
Paid time off
401(k) plan with employee and company contribution opportunities
Life insurance
Disability insurance
Accident insurance
Tuition reimbursement
Potential eligibility for performance-based incentive compensation, which may include cash bonuses and/or long-term incentives
Professional development opportunities