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Bachelor's in STEM Virtual Hiring Event

Medpace Holdings, Inc.

United States, OH, Cincinnati | United States, TX, Irving (Dallas)

Job Summary

Candidates with Bachelor's Degrees in STEM - join us virtually on March 2nd to learn about our available positions in Data Management and Biostatistics.

Medpace will be hosting a Virtual Hiring Event regarding our opportunities for Bachelor's Degrees in our Cincinnati, OH and Dallas, TX offices.

WHEN: Thursday, March 2nd, 2023 at 5:00 PM EST.

If interested, please fill out an application below. More details regarding the format of the event will be provided should you be selected to attend. We're excited to speak to you!

Responsibilities

Below are the positions that will be represented at the event:

eClinical Coordinator

  • Partner with eClinical Managers and Sponsors to develop and configure device applications unique to each study’s needs
  • Support management of device inventory and oversee global shipping and distribution of devices to study sites
  • Develop device and application user guides and troubleshoot issues by working with sites/sponsors, as necessary

RSP Coordinator

  • Manage logistics of study product shipments
  • Work with international clients in obtaining requirements and responding to inquiries
  • Create study specific documents
  • Working knowledge of Excel

Data Coordinator

  • Validate an entry database design
  • Clean the clinical database, which includes generating and resolving data clarifications
  • Perform QC audits of the clinical database
  • Report metrics and data trends on projects

SAS Programmer

  • Program edit checks for external data
  • Integrate external data with the mapped database
  • Coordinate communication with Data Manager, Biostatistician, and/or external database providers regarding database specifications and data transfers

Clinical Database Programmer

  • Develop, program, validate and maintain clinical trial electronic data capture (EDC) databases according to company standards;
  • Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards;
  • Perform integration testing to QC the database;

IRT Programmer/Validator

  • Review of validation packages created by other team members;
  • Review requirement specification documents provided by internal clients; and
  • Validation of new projects and changes to existing projects;

Clinical Data Analyst

  • Develop data visualization specifications that meet client needs
  • Using Spotfire; Develop data visualization dashboards and reports
  • Communicate and present data visualization dashboards and reports to internal and external clients

Project Coordinator - Data Monitoring

  • Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials
  • Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes)
  • Assist in the development and maintenance of study specific documents describing DMC processes and procedures

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

Project Coordinator - Imaging

  • Compile and maintain project-specific status reports and project timelines associated with Imaging studies;
  • Maintain inventory of imaging supplies for study sites; and
  • Interact with study sites and internal associates.

Project Coordinator - Data Monitoring

  • Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials
  • Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes)
  • Assist in the development and maintenance of study specific documents describing DMC processes and procedures

Qualifications

  • Graduating seniors (May 2023) with Bachelor's in STEM
  • currently hold a Bachelor's in STEM
  • 3.0 GPA or higher
  • Willing to relocate to Cincinnati or Dallas

Job posted: 2023-02-08

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