Research Coordinator

Responsibilities

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, ensure 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 participants

Conduct participant research visits and collect/record research related data. Submit data to study sponsors as required and document in the participant’s study chart as appropriate. Maintain the integrity and privacy of participant’s research protocol chart with all required source data

Demonstrate accuracy and organizational skills and the ability to follow through on requests and meet timelines. Communicate with study team and supporting clinical groups in professional and clear manner to support study activities

Assist with documentation and submission for approvals, revisions, renewals, informed consents, unanticipated problems, and study closure as mandated by the study sponsors, St. Elizabeth Healthcare, and the Institutional Review Board (IRB)

Obtains patient biologic specimens or works with SEH laboratory/SEH clinical nursing staff to obtain laboratory specimens (blood, urine, saliva, etc.). Maintains IATA certification for the safe handling and shipping of biologic specimens

Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors

Performs other duties as assigned

Benefits

Competitive pay

Comprehensive health coverage within the first 30 days

Generous paid time off

Flexible work schedules

Retirement savings with employer match

Tuition reimbursement

Professional development opportunities

Wellness programs

Mental health programs

Recognition programs

Career advancement through mentorship and internal mobility

Glassdoor

3.9

St. Elizabeth Healthcare is one of the oldest, largest and most respected medical providers in the Greater Cincinnati region.

Edgewood, Maryland, USA

http://www.stelizabeth.com/

Late Stage

Leadership Team

Bruno Giacomuzzi, FACHE

Senior Vice President and Chief Operating Officer

James Horn, MD, MBA, FACEP, LSSBB

EVP/Chief Clinical Officer

Recent News

Morningstar.com

WellCare of Kentucky recognizes 2026 Community Health Champions

2026-09-10

EIN Presswire

CardioRenal Systems Secures FDA IDE Approval and Strategic Hospital Investment

2026-07-07

Lane Report | Kentucky Business & Economic News

Qualifications

Associate degree in related field with 2 years related experience

Bachelors degree in related field

Understanding of research processes

Required skills

Represents the skills you have, click on the tags

Experience

2+ years