Why Summit Medical Group
FY2024 · Form 990Its mission and biggest programs, as filedProvides quality medical care to all patients, regardless of ability to pay.
- Summit Medical Group, INC. DBA st. Elizabeth physicians ("sep") is a multi-specialty physician organization dedicated to physician directed delivery of quality Medical care in the northern kentucky, southwestern ohio, and southeastern indiana areas. St. Elizabeth physicians and associates are patient…$454.5M spent in FY2024
Before you apply
FY2024 · Form 990Independent: from IRS data, not the orgAbout the role
The org's own posting, as writtenEngage with us for your next career opportunity. Right Here. Job Type: Regular Scheduled Hours: 40 💙 Why You’ll Love Working with St. Elizabeth Healthcare At St. Elizabeth Healthcare, every role supports our mission to provide comprehensive and compassionate care to the communities we serve. For more than 160 years, St. Elizabeth Healthcare has been a trusted provider of quality care across Kentucky, Indiana, and Ohio. We’re guided by our mission to improve the health of the communities we serve and by our values of excellence, integrity, compassion, and teamwork. Our associates are the heart of everything we do. 🌟 Benefits That Support You We invest in you — personally and professionally.
Enjoy: - Competitive pay and comprehensive health coverage within the first 30 days. - Generous paid time off and flexible work schedules - Retirement savings with employer match - Tuition reimbursement and professional development opportunities - Wellness, mental health, and recognition programs - Career advancement through mentorship and internal mobility Job Summary: Coordinate clinical research studies for the principal investigators and coordinates and promotes research program within St. Elizabeth and the community. Responsible for networking with physicians to open studies, educating staff about current studies, educating clients about studies and obtaining informed consents.
Responsibilities include screening and enrolling subjects in studies and managing their participation according to ethical, regulatory, and protocol specific requirements. Responsibilities also include data collection and submission as well as Regulatory compliance. Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background.
Job Description
Coordinate clinical research studies conducted by the principal investigator. Perform study conduct in accordance with the protocol, manual of operations, and standard operating procedures (SOPs). Collaborate with physicians to open new studies at St. Elizabeth and to promote the research program within the community. Work directly with principal investigator to assist in the design of recruitment strategies, communication plan, patient safety monitoring plan, e nsure compliance with protocol guidelines and requirements of regulatory agencies, including required documentation and record retention. Assist in coordinating study documents for review by the IRB and Sponsor.
Conducts research studies according to Office for Human Research Protections (OHRP) and US Food and Drug Administration (FDA) regulations and guidelines. Follows Good Clinical Practices, Good Laboratory Practices, St. Elizabeth Healthcare policies, and maintains related certifications. Identify or assist in the screening of potentially eligible participants. Consent participants and coordinate, plan and execute study visits and provide instructions and reimbursement to…
About Summit Medical Group
From its Form 990- Budget $548.3M · Health Care
- Staff 2,506 · founded 1995
- Pays its leaders $515K–$1.6M (12 reported)
- Open jobs 300 · Jobs at Summit Medical Group · Full 990 report