Feasibility Coordinator
MEDPACE
Warsaw, Poland
‎11 godz. temu

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

We are currently seeking a Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross functionally with our clinical operations, medical and regulatory submissions teams, as well as through obtaining direct feedback from investigative sites, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials.

If you are an individual with a clinical background and expertise in clinical research, please review the following career opportunity.

Responsibilities

  • Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams;
  • Develop preliminary proposal strategy for site and country selection;
  • Perform outreach to investigative sites to obtain indication and protocol specific feedback;
  • Present feasibility results to members of the proposal team to assure correct assumptions were applied and strategy is in line with our therapeutic and operational experience;
  • Create study-specific feasibility questionnaires, cover letters, and other feasibility-related documents;
  • Assist project teams with preparation for bid defense meetings; and
  • Support departmental process improvement initiatives and general departmental administrative functions.
  • Qualifications

  • Bachelors degree in life sciences required, Masters or PhD preferred;
  • At least two years of clinical research experience;
  • Analytical thinker with great attention to detail;
  • Ability to prioritize multiple projects and tasks within tight timelines;
  • Working knowledge of feasibility processes; and
  • Excellent written and verbal 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 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
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