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Medpace Jobs in Cold Spring, KY (NOW HIRING)

Radiologist - Core Laboratory

Cincinnati, OH · On-site

$307K - $384K/yr

Completing source documents accurately and promptly, according to the specific protocol requirements and Medpace's SOP * Blinded independent central review of radiology examinations according to ...

Job Summary Medpace is seeking experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to ...

Job Summary Medpace is seeking entry-level finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to ...

Senior Finance Account Analyst

Cincinnati, OH · On-site

$82K - $102K/yr

Job Summary Medpace is seeking experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to ...

Job Summary Medpace is seeking experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to ...

Provide nursing coverage as required for the Medpace Clinical Pharmacology Unit according to the study protocol, applicable SOPs, and Good Clinical Practice; * Perform and document clinical ...

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Medpace information

See Cold Spring, KY salary details

$10

$58

$95

How much do medpace jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for medpace in Cold Spring, KY is $58.43, according to ZipRecruiter salary data. Most workers in this role earn between $47.88 and $66.15 per hour, depending on experience, location, and employer.

Is Medpace a legit company?

Medpace is a reputable global contract research organization (CRO) that provides clinical development services for the pharmaceutical and biotech industries. It is known for its compliance with industry standards and regulatory requirements, making it a legitimate employer in the clinical research field.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Medpace, and why are they important?

To thrive as a Clinical Research Associate at Medpace, you need a solid background in life sciences or a related field, experience in clinical trials, and strong knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and possibly certifications like SOCRA or ACRP are typically required. Excellent organizational skills, attention to detail, and effective communication are crucial soft skills for managing study sites and collaborating with diverse teams. These competencies ensure the integrity of clinical trials, regulatory compliance, and successful project outcomes.

What are some common challenges Clinical Research Associates (CRAs) face at Medpace, and how does the company support their professional development?

Clinical Research Associates at Medpace often encounter challenges such as managing multiple clinical trial sites, ensuring regulatory compliance, and maintaining clear communication with both site staff and internal teams. Medpace supports its CRAs through structured onboarding, ongoing training programs, and mentorship from experienced professionals. The company also encourages career growth by providing clear advancement paths and opportunities to specialize in various therapeutic areas or move into project management roles.

What benefits does Medpace offer employees?

Employees at Medpace typically receive a comprehensive benefits package that includes health insurance, retirement plans, paid time off, and professional development opportunities. The company also offers wellness programs and flexible work arrangements to support employee well-being and work-life balance.

What degree gets you a job at Medpace?

For roles at Medpace, including clinical research associates and scientists, a bachelor's degree in life sciences, healthcare, or related fields is typically required. Advanced positions may require a master's or doctoral degree, along with relevant certifications and experience in clinical research or regulatory affairs.

What exactly does Medpace do?

Medpace is a global contract research organization (CRO) that provides clinical trial management and research services for the pharmaceutical, biotech, and medical device industries. Employees in this field typically coordinate study protocols, ensure regulatory compliance, and support data collection using specialized tools and industry standards. The role often requires knowledge of clinical research processes and relevant certifications.

What is Medpace and what does the company do?

Medpace is a global, full-service clinical contract research organization (CRO) that provides services to the biotechnology, pharmaceutical, and medical device industries. The company specializes in the design and management of clinical trials to help bring new drugs and medical devices to market. Medpace offers a range of services, including regulatory consulting, clinical trial management, data management, and biostatistics. Their work is critical in ensuring that new therapies are safe and effective for patients.
Nurse Practitioner - Diabetes & Endocrine

Nurse Practitioner - Diabetes & Endocrine

Medpace

Cincinnati, OH • On-site

Other

Medical, PTO

Re-posted 24 days ago


Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

14th of 59 rated research


Job description

Nurse Practitioner

We are seeking Nurse Practitioners with diabetes or endocrine experience to join our dynamic team. In this role, you will work side by side with our physicians, serving as a clinical expert, to support our project teams in clinical research studies. If you are interested in contributing to innovative clinical research in a highly collaborative environment, this is the right opportunity for you.

Responsibilities
  • Develop and implement disease-specific and clinical education for internal teams
  • Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team
  • Review assigned protocols for scientific and participant safety matters and risks
  • Attend pre-study and study-related meetings with project teams, providing clinical expertise
  • Assist the Clinical Operations team with activities related to study participant recruitment, screening and study conduct
  • Participate in new business activities by providing clinical input in Medpace's written proposals for conducting a client's clinical trial
  • Serve as a clinical expert in business presentations to new clients
Qualifications
  • Masters or doctorate degree;
  • Active Nurse Practitioner license;
  • At least 1-2 years of clinical experience as a Nurse Practitioner specializing in diabetes/endocrine patient care
  • Prior clinical research experience preferred; and,
  • Experience working with adult or pediatric populations using continuous glucose monitors (CGMs) preferred.
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.


What Medpace employees say

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Benefits

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992