This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Entry Level Recruitment Event and Open House - April 18th

Medpace Holdings, Inc.

United States, OH, Cincinnati | United States, OH, Cincinnati

Job Summary

Medpace will be hosting a Cincinnati In-Person Recruitment Event.

WHEN: April 18th 5:00pm EST

**More details regarding the location of the event will be provided should you be selected to attend.


Below are the positions we will be recruiting for at this event:

Clinical Research Associate

  • Comprehensive training program that will provide you the resources and knowledge to monitor sites independently
  • Must be willing to travel 60-70%
  • Communicates with medical staff and clinical research physicians

Patient Recruitment Coordinator

  • Implement various recruitment strategies for clinical research studies
  • Work effectively with the Clinical Research Associate (CRA) to discuss recruitment strategies and enrollment targets
  • Work effectively with Recruitment to develop recruitment plans and ideas for new and on-going studies

Project Coordinator

  • Partner with Clinical Trial Manager to coordinate daily study activities
  • Central point of contact for internal and external team members
  • Create and maintain project timeline

Regulatory Submissions (Study Start-Up) Coordinator

  • Assist with the start-up of clinical research sites
  • Collaborate with Institutional Review Boards (IRBs)
  • Prepare regulatory documents, including Informed Consent Forms

Data Coordinator

  • Participate as part of a team on various projects
  • Validate an entry database design
  • Report metrics and data trends on projects
  • Identify data conflicts and issues on projects

Data Standard Analyst

  • Create annotated CRFs per CDISC SDTM standard and mapping specifications for study level data collection source data to CDISC SDTM
  • Implement data standard and create SDTM data
  • Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents

eClinical Coordinator

  • Work with vendors to ensure patient forms meet their respective electronic requirements
  • Partner with Sponsors to develop application requirements for each unique study, which involves setting up application with appropriate questions from validated questionnaire library (e.g., SF-36, or creating specific diary type questions)
  • Assist in the creation and maintenance of metric reports and study specific documents (e.g.,Site Reference Guide, Study Screenshots)

Proposal Writer

  • Manage proposal development process for new business
  • Strategize content across science, finance, and operations

Quality Assurance

Junior Business Intelligence Analyst

  • Gain experience and exposure to advanced BI conceptsfrom visualization to data warehousing
  • Grow business knowledgeby working with leadership across all aspects of Medpace’s business

Site Payments Processor

  • Responsible for the daily execution of accounts payable and Site Payment data entry activities for assigned studies
  • Manage the setup of system requirements to track and administer site payments
  • Manage the processing/calculation of site payments

MBL Lab Technician

  • Prepare samples according to project protocol and/or related SOPs;
  • Maintain compliant laboratory documentation;
  • Perform data analysis and data checking;
  • Interpret results obtained for accuracy and acceptability


  • Create and maintain laboratory manuals (general and study-specific) and other study- related documents;
  • Develop and present clinical laboratory presentations at investigator meetings;
  • Design specifications and monitor production of specimen collection kits;

Graphic Designer

  • Design resonating brand identities and creative materials (e.g., brochures, flyers, handbooks) for clinical studies
  • Collaborate across roles to visualize complex concepts, communicate tone, and achieve the client’s vision
  • Provide design expertise to other areas of the company, including support for new business presentations, promotional materials, and digital assets for web and email

Technical Writer/Instructional Designer

  • Empower learners to excel in their roles by producing effective training materials and e-learnings
  • Translate complex ideas into clear and concise help documentation for proprietary Medpace clinical trial software
  • Increase document usability by applying design standards to templates and forms

Print Production Specialist

  • Evaluate and prioritize internal print requests
  • Print and assemble creative materials for clinical studies (e.g., brochures, flyers, handbooks)
  • Communicate with staff about print requests and coordinate approval for quotes and proofs

Design Coordinator

  • Design and format clinical study materials (e.g., worksheets, informational cards, questionnaires) for patients, caregivers, research site staff, and physicians
  • Incorporate amendments and translations into existing documentsusing Adobe InDesign, Adobe Illustrator, and Microsoft Word;

  • Manage translations to deliver high-quality materials around the globe

Positions located in Cincinnati


  • Minimum of Bachelor's degree in Life Science Field; Advanced degree preferred
  • Previous experience in a clinical research setting
  • 3.0 GPA or higher

Job posted: 2023-03-17