Entry Level Recruitment Event and Open House - April 18th

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

MRL Lab PC

• 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