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Medpace, Inc. logo

Clinical Nurse Study Coordinator

Medpace, Inc.·Cincinnati, Ohio

Full Time·Hybrid·0-2 yrs·Posted 28 days ago
Practice for this role

About the role

The Clinical Nurse Study Coordinator is responsible for the accurate administration of medications, monitoring of adverse events, and performing clinical procedures according to study protocols. They also collaborate with project managers and investigators to ensure operational flow and data integrity.

Are you a Registered Nurse looking to expand your clinical career beyond traditional bedside nursing? Medpace is seeking a Clinical Nurse Study Coordinator to join our Clinical Pharmacology Unit (CPU), where nurses play a critical role in the development of new medicines and therapies. In this role, you will work directly with study participants, physicians, and clinical research professionals while gaining experience in Phase I clinical trials. This position offers a great opportunity to combine patient care, clinical research, and career growth to directly contribute to advancing innovative therapeutics.

Responsibilities

May assist in interviewing, evaluating, and scheduling prospective study subjects according to protocol criteria; Responsible for accurate and safe administration of medications according to protocols; Responsible for assessing subjects for adverse events and ensuring they are documented; Perform and/or schedule procedures (e.g. vital signs, intravenous insertions, venipunctures, laboratory tests, ECGs, etc.); Work closely with Project Managers on operational matters (i.e. study execution planning, operational flow); Interacts with study Monitors and resolving data queries, confirming eligible subjects, and interacting with the Investigator for medical matters.

Qualifications

Bachelor's degree, nursing license (RN); Clinical experience in acute care setting preferred. Why Nurses Choose Clinical Research Structured daily schedule Opportunity to participate in the development of future therapies Continued use of nursing skills while learning and growing professionally Collaborative, team-based environment

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO).

We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People.

Purpose.

Passion.

Make a Difference Tomorrow.

Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.

The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Requirements

Candidates must hold a Bachelor's degree and a valid nursing license (RN). Previous clinical experience in an acute care setting is preferred.

  • bachelor degree
  • Venipuncture
  • Nursing
  • ECG
  • Vital signs monitoring
  • Medication administration
  • Laboratory testing
  • Clinical research
  • Intravenous insertion
  • Patient interviewing
  • Study coordination
  • Clinical pharmacology
  • Data query resolution
  • Study protocol compliance
  • Adverse event assessment

Benefits

  • Competitive compensation
  • Flexible work hours
  • On-site fitness center
  • Employee appreciation events
  • Community involvement
  • Health and wellness initiatives
  • Onsite childcare
  • Competitive PTO packages
  • Discounted tuition for UC online programs
  • Discounts on local sports games
  • Structured career paths
  • Discounts on local fitness gyms
  • On-site bar and restaurants

Posting details

Employment type
Full Time
Work arrangement
Hybrid
Experience
0-2 yrs
Location
Cincinnati, Ohio
Posted
Jun 29, 2026
Closes
Apr 6, 2027
Application
Employer website
Medpace, Inc. logo

Hiring organization

Medpace, Inc.

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development...

IndustryPharmaceutical Manufacturing
TypePublic Company
Size5,001-10,000 employees
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