live chat
Cincinnati Clinical Research Project Coordinator Job in Cincinnati, Ohio US
Monster
 
 
 
 

Job Summary

Company
Medpace, Inc.
Location
Cincinnati, OH
Industries
Government and Military
Job Type
Full Time
Employee
Years of Experience
Less than 1 Year
Job Reference Code
40574430_2

Cincinnati Clinical Research Project Coordinator

About the Job

Cincinnati Clinical Research Project Coordinator



Job Locations

United States-OH-Cincinnati






Category


Clinical Operations



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 approximately 3,500 people across almost 40 countries.



Job Summary





We are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management 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 can use your previous clinical research expertise and develop your career even further, then this is the opportunity for you.



Responsibilities





Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Create and maintain project timelines; and
Coordinate project meetings and produce quality minutes.



Qualifications





Bachelor's degree in a health sciences field;
Prior experience as a Study Coordinator or within the pharmaceutical industry; and
Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.



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 historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

*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.



Need help finding the right job?




We can recommend jobs specifically for you!
Click here to get started.


EO/AA Employer M/F/Disability/Vets
 

Job Tools

  • Save
  • Share
  • Report this job