Clinical Project Manager
MEDPACE
London, United Kingdom
1d ago

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 approximately 3,500 people across almost 40 countries.

Job Summary

Position : Clinical Trial Manager (Clinical Project Manager)

London, office-based (flexible-remote working due to Covid-19 restriction)

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;
  • Strong experience in project management / clinical trial management in clinical research industry;
  • Strong leadership and influencing skills; and
  • 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 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
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