Clinical Trial Manager

Job Description

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 2,700 people across 36 countries.

Job Summary

Clinical Trial Manager (Clinical Project Manager)

Permanent

Location: office based in London or Stirling; or home based anywhere in UK

Salary: competitive, plus car allowance, bonus, generous benefits package

Responsibilities

Medpace is currently looking for Clinical Trial Managers (CTMs) to lead clinical research studies. The CTM position performs as project lead for multiservice full service global clinical trials.

The position interacts with sponsors, manages the timeline and all project deliverables, and coordinates all services contracted for the study. CTMs are also responsible for leading a team of CRAs and managing project coordinators.

Our full-service approach is led by medical, regulatory and operational experts with deep therapeutic experience. The disciplined processes, site relationships, and technologies enable CTMs to execute even the most complex global studies. Therapeutic focus areas including oncology, cardiovascular, endocrine/metabolic, infectious disease, CNS. Trials include those in rare disease and Advanced Therapies.

The Medpace full service offering, advanced cross functional integrated CTMS (Clinical Trial Management System), and clearly defined empowered clinical trial management structure ensures focus on the operational execution of the project, versus excessive time being spent on project financial tracking.

Qualifications

• Bachelor’s degree in a health related field; Advanced degree in a health related field preferred
• Previous experience in project management/clinical trial management in clinical research industry
• Strong leadership and influencing skills
• Excellent planning, organisation, prioritisation 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 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.