Nursing Clinical Research Opportunities

Job Locations United States-OH-Cincinnati
Category
Clinical Operations

Overview

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 of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 3,000 people across 36 countries.

Job Summary

Project Coordinator

 

As a Project Coordinator, you will have the opportunity to work within our Clinical Trial Management group, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with the clinical trial management team, you will gain valuable hands on experience to enable you to develop a career in clinical research.

 

Responsibilities

  • Responsible for routine departmental support including maintaining supplies, shipping, archiving, filing, faxing, scheduling meetings, and providing minutes
  • Maintain departmental databases and electronic clinical trial registries
  • Obtain certifications for official study documents

Qualifications

  • Bachelor's Degree in a health science field
  • Excellent computer, organizational, and communication skills

 

Regulatory Submissions Coordinator

 

Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. 

 

Responsibilities 

  • Communicate with research sites regarding the distribution and review of site essential documentation
  • Maintain and perform quality review of Trial Master File (TMF)
  • Collect, review, organize, and assemble regulatory start-up submissions
  • Maintain timelines for site start-up
  • Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements
  • Review pertinent regulations and guidance to develop proactive solutions to regulatory submissions issues and challenges

Qualifications

  • A minimum of a Bachelor's degree is required (preferably in a Life Sciences field)
  • Some experience in an office setting is preferred
  • Excellent organizational and prioritization skills
  • Knowledge of Microsoft Office
  • Great attention to detail and excellent oral and written communication skills

 

Clinical Research Associate 

 

The Clinical Research Associate position at Medpace is a unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

 

Responsibilities 

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating  protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
  • Verification that the investigator is enrolling only eligible subjects;
  • Regulatory document review;
  • Medical device and/or investigational product/drug accountability and inventory;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  • Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

  • Must have a minimum of a Bachelor’s degree in a health or science related field;
  • Ability to travel 60-80% to locations nationwide is required;
  • Must maintain a valid driver’s license and the ability to drive to monitoring sites;
  • Minimum 1 year healthcare-related work experience preferred;
  • Proficient knowledge of Microsoft® Office;
  • Strong communication and presentation skills; and
  • Must be detail-oriented and efficient in time management.

Responsibilities

See above for responsibilities of PC, RSC, and CRA.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities. 

 

Awards

  • Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer
  • Winner of the ACRP-Avoca CRO Quality Award in 2018
  • Recognized with six CRO Leadership Awards from Life Science Leader magazine
  • Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships

 

What to Expect Next

We look forward to receiving your application.  A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.

 

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*WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money.  These scammers pose as legitimate employees from actual companies.  Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

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