Clinical Research Coordinator

Responsibilities

Demonstrates the ability to develop processes to facilitate implementation of the research protocol to provide effective and safe medical research to all subjects. Demonstrates the ability to identify potential and/or actual issues which may prohibit the accurate implementation of the research protocol and initiate interventions to avoid protocol violations and /or unsafe practice. Demonstrates the ability to coordinate necessary activities between Study Coordinators and the Principal Investigator

Performs initial and ongoing evaluations of research subjects and implements care directed towards optimal outcomes. Plans care for research subjects/family based on clinical consultation, standards of care, optimal outcomes and protocol requirements. Implements and evaluates plan of care. Performs technical skills according to policy and procedure and accepted TriHealth standards. Documents in medical record appropriately

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with IRB/FDA standards and deadlines in completing Progress Reports. Assures compliance with IRB/FDA standards and deadlines in reporting all deaths and adverse events with study subjects. Assures compliance with IRB/FDA standards and deadlines in facilitating communication between study sponsor and designated TriHealth IRB

Assesses potential subjects for inclusion and exclusion criteria. Keeps Case Report Forms complete and thorough using the IRB and FDA standards. Supports hospital staff in complying with research protocols and works to minimize the impact on their workload. Keeps queries and protocol violations that can be controlled to a minimum. Responds appropriately and accurately to all queries in a timely fashion. Maintains accurate and detailed follow up schedules to assure meeting regulatory time points

Demonstrates knowledge of available studies, screening potential patients for eligibility, guiding physicians and staff in needed timetables for capturing protocol related data points. Attends trainings required by sponsoring organizations for specific protocols and/or attends meetings related to the initiation or on-going progress of a sponsored clinical trial. Acts as the point person for audit staff coming into institution for a review prepares a written response with a plan of action to any major/minor deficiencies

Benefits

Competitive shift differentials

Opportunities for professional growth

A comprehensive benefits package that may include medical, dental, vision, paid time off, retirement savings plans, and tuition reimbursement

Glassdoor

3.7

TriHealth is a unified health system based in Cincinnati, Ohio, United States.

Cincinnati, Ohio, USA

http://www.trihealth.com

Late Stage

Total Funding

unknown

Key Investors

American Society for Clinical Pathology

2026-07-20

Grant

Leadership Team

John Ward

Chief Operating Officer

Donna Peters

Senior Vice President & Chief Information Officer

Recent News

Bizjournals.com Feed (2025-11-12 15:43:17)

TriHealth's first female CEO in rare company in helming $3B healthcare system

2026-07-03

Morningstar.com

AAHRPP Accredits Five More Research Entities

2026-07-01

TriHealth fills key C-suite role from within as new CEO takes the helm

2026-06-17

Company data provided by

Qualifications

Bachelor's Degree in Biological Science; Hard Sciences, Psychology, Sociology

Equivalent experience accepted in lieu of degree

Basic Life Support for Healthcare Providers (BLS)

Required skills

Represents the skills you have, click on the tags, Basic Life Support (BLS)

Experience

Mid level