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Job Details

Project Coordinator - Medical Device

Company: Medpace
Location: Blaine, Minnesota, United States, 55014
Reference: 103313485
Closing Date: 07 Aug 18
Type: Not Specified
Salary (£): Competitive
Benefits:

Job Summary:

United States-MN-BlaineCategory Medical DevicePosition Type Full-TimeOverviewMedpace 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 dee...

Requirements:


United States-MN-Blaine

Category Medical Device
Position Type Full-Time


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 2,500 people across 35 countries.

We are currently seeking a full-time, office-based Project Coordinator to join our Medical Device team in Blaine, MN. 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

  • Maintain effective and efficient sponsor communication, identify and anticipate possible issues or challenges, and work as a team to develop appropriate solutions;
  • Daily clinical site activity such as site initiation, product training, study enrollment, study metrics tracking and reporting, clinical data flow, site monitoring, and site close-out;
  • Ensure the validity of the clinical study data through error checking and facilitation of error resolution, as well as implement and educate on study specific procedures; and
  • Assist in the development of protocols, Case Report Forms, Data Management Plans, Monitoring Plans and other study specific procedures, as well as provide forecast and budget support and provide onsite monitoring of clinical records, as appropriate.


Qualifications

  • Bachelor's degree in Life Sciences or a related field and at least 6 months of research experience post graduation;
  • Outstanding oral and written communication skills;
  • Ability to interact with medical personnel and attend medical procedures;
  • Ability to work well in a team environment;
  • High attention to detail and quality standard; and
  • Proficient in Microsoft Office applications
  • Clinical study experience, including prior experience with medical devices and IDE trials preferred.


Travel: None

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 and 2017 by the Cincinnati Enquirer
  • Winner of the ACRP-Avoca CRO Quality Award in 2018
  • 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.

EO/AA Employer M/F/Disability/Vets

*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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Apply for this job: Project Coordinator - Medical Device

Contact Information:

Address:  Medpace, Inc
5375 Medpace Way
Cincinnati
Ohio
45227
USA
Tel:  +1 513 579 9911
Fax:  +1 513 579 0444
Website:  Visit Our Web Site

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