Academic Research Coordinator

TriHealth•Cincinnati, OH

1d•Onsite

About The Position

Join TriHealth as an Academic Research Coordinator! At TriHealth, you’ll join a nationally respected, mission‑driven health system where your work directly advances clinical discovery and improves patient outcomes. As an Academic Research Coordinator within the Hatton Research Institute, you’ll coordinate and manage all aspects of clinical trials with a strong focus on safety, integrity, and regulatory excellence. You’ll collaborate closely with PIs, multidisciplinary teams, and external partners while maintaining high‑quality study data, ensuring IRB/FDA compliance, supporting subject enrollment, and contributing to protocol development, feasibility assessments, and scientific presentations. This role is ideal for research‑minded professionals who bring a bachelor’s degree in science, 2–3 years of healthcare experience, strong organizational skills, and proficiency in Microsoft Office. At TriHealth, you’ll be supported by a culture that values teamwork, professional growth, and meaningful impact. You’ll play a key part in advancing innovative research while working in an environment known for its commitment to excellence and its people. Apply today and grow your career with a team that truly values you.

Requirements

Bachelor's Degree in Science (Required)
2 - 3 years’ experience Professional Healthcare (Required)
Microsoft Office
Basic Life Support (BLS) Upon Hire Required

Responsibilities

Develops 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.
Ensure compliance with IRB/FDA standards and deadlines in the following: notification of subject randomization and enrollment, completing Progress Reports, reporting all deaths and adverse events with study subjects, and 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.
Maintains study data and performs intermittent analysis.
Responsible for working with the PI and study team to determine correct study design, perform literature searches, protocol writing and development, and feasibility assessment.
Serves as the contact for all internal and external customers, including external compounding pharmacies, with knowledge of external pharmaceutical regulations.
Maintains study data and performs analysis; and assists with study presentation materials and developing posters for presentation and / or manuscript for publication.
Develop preliminary study budgets. Potentially works with the IACUC and process for CME application.
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 records appropriately.