Clinical Project Coordinator - Stirling, United Kingdom - Medpace, Inc.

Medpace, Inc.
Medpace, Inc.
Verified Company
Stirling, United Kingdom

1 month ago

Tom O´Connor

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Tom O´Connor

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Description

Job Summary:

Position:
Project Coordinator

Location:
Office-based, Stirling

Overview:
This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, NHS or Clinical Trials experience is also beneficial


Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing UK team and engage in clinical trial management on a day to day level.

This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company's success.


Responsibilities:

  • Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy;
  • Compile and maintain projectspecific status reports within the Clinical Trial Management System (CTMS);
  • Interact with the internal project team, Sponsor, study sites, and thirdparty vendors;
  • Ownership of the Trial Master File;
  • Create and maintain project timelines and enrolment projections; and
  • Coordinate project meetings and produce quality minutes.

Qualifications:

  • Bachelors' Degree in Life Sciences, Master's Degree preferred;
  • Excellent oral and written English Language communication skills;
  • Knowledge of Microsoft Office programs;
  • Experience in a health sciences or business setting preferred;
  • Excellent organisational and prioritisation skills;
  • Strong attention to detail.

Medpace Overview:
Medpace is a full-service clinical contract research organisation (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 5,000 people across 40+ countries.


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.


Perks (

_vary by location and position_

):

  • 25 days paid holiday (+bank holidays)
  • Flexible working
  • Private Medical Insurance & Dental Insurance
  • Company Pension Scheme
  • Life Insurance
  • Eye care scheme

Awards:


  • Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Recognized by Forbes as one of America's Best Midsize Companies in 202
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organisation, 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.


  • EO/AA Employer M/F/Disability/Vets_
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