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Entry Publishing Associate

Overview

Medpace is a full-service clinical contract research organization (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

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Publishing Associate to join our Regulatory Affairs team. 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

  • Publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, eCTD, and other applicable electronic publishing standards;
  • Implement publishing processes across multiple complex regulatory documents;
  • Perform document quality control checks for others in the department, promptly communicating irregularities in documents and coordinating issue resolution;
  • Assist Medical Writers in the development and compilation of appendices of Clinical Study Reports;
  • Provide day-to-day department support activities as necessary to aide completion of documents, including Clinical Study Reports, Report Appendices, Protocols, etc.;
  • Support management with the conduct of procedural and software training
  • Develop understanding and maintain knowledge of appropriate standard operating procedures (SOPs), regulations, policies, and regulatory guidance documents; and
  • May be responsible for other projects and responsibilities as assigned

Qualifications

  • Bachelor’s Degree required;
  • Experience or willing to learn publishing tools: Adobe, Global Submit, etc;
  • A rapid increase in eCTD document structure, system, & content knowledge is expected;
  • Demonstrates a high attention to detail and the ability to successfully train & learn under the more advanced Specialists on how to conduct all quality assurance reviews in the specified areas required for document finalization; and
  • Employee will be expected to increase communication skills and the ability to work with a diverse group of people.

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
  • Recognized by Forbes as one of America's Best Mid-size Companies in 2021
  • 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