Inova Health is looking for a dedicated Project Manager to join the team. This role will be full-time day shift from Monday - Friday, 8:00 a.m. - 4:30 p.m., Onsite
The Project Manager assumes responsibility for implementing new programs and initiatives. Provides direction and supervision of all newly established programs and processes where required. Provides workflow analysis and documentation for the Medical Management department, outpatient/inpatient, case/disease management, special populations, vendor management, denial process, and assessment of the contract requirements for all services. Works closely and collaboratively with other Inova Health System team members and leadership.
Inova is consistently ranked a national healthcare leader in safety, quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.
Featured Benefits:
Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program. Retirement: Inova matches the first 5% of eligible contributions – starting on your first day. Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans. Mental Health Support: offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost. Work/Life Balance: offering paid time off, paid parental leave, and flexible work schedules
Project Manager Job Responsibilities
Minimum Requirements
Experience - 2 years of management experience and 5 years of Project Management experience
Education - Bachelor’s degree in relevant field (or 4 years of experience in lieu of degree)
Preferred Requirements
Demonstrated experience coordinating and managing clinical trials, including patient scheduling, informed consent, data collection, and regulatory documentation. Hands-on experience interacting with and seeing patients for clinical trial activities, ensuring high-quality patient care and compliance with study protocols. Strong background in clinical research operations and regulatory requirements. Proven ability to conduct and support research activities, including literature reviews, protocol development, and data analysis. Experience working across diverse teams and disciplines, such as physicians, nurses, data managers, and statisticians. Exposure to multiple therapeutic areas and disease groups, with flexibility to adapt to varying protocols and study requirements.