Medpace Networking Event at University of Cincinnati

Medpace, Inc.•Cincinnati, OH

7d•Onsite

About The Position

Medpace will be hosting an In-Person Networking Event at the University of Cincinnati for upcoming graduates! WHEN: April 21st at 6:00 PM EST WHERE: University of Cincinnati More details regarding the format of this event will be provided should you be selected to attend Responsibilities Below are the positions we will be recruiting for at this event: Clinical Data Coordinator: Validate entry database designs Report metrics and data trends on projects Identify data conflicts and issues on projects Work with personnel from global research sites to resolve data conflicts Clinical Project Coordinator 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 Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout Clinical Research Associate Comprehensive training program that provides resources and knowledge to monitor sites independently Travel to non-local, national study sites 60-80% of the time Communicate with medical staff and clinical research physicians on site Data Engineer: Utilize skills in development areas including data warehousing, business intelligence, and databases (Snowflake, ANSI SQL, SQL Server, T-SQL) Support programming/software development using Extract, Transform, and Load (ETL) and Extract, Load and Transform (ELT) tools, (dbt, Azure Data Factory, SSIS) Design, develop, enhance and support business intelligence systems primarily using Microsoft Power BI Patient Recruitment Coordinator Implement various recruitment strategies for clinical research studies; Work with the sites, CTM and Clinical Research Associate to discuss recruitment strategies and enrollment targets Develop recruitment plans and ideas for new and on-going studies Project Coordinator - CRO 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 Coordinator Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF) Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards) Software Engineer/Software Development Co-Op Build software applications and features in an Agile environment by following our software development lifecycle (SDLC) process Develop applications in a hybrid and cloud native setting utilizing development skills that include object-oriented programming (C#), databases (SQL), Entity Framework (EF), Angular, and web applications (ASP.NET) Participate in requirements gathering, design, development, testing, release, and support of applications

Requirements

3.3-3.5 GPA or higher
Willing to work office-based in Cincinnati, OH

Responsibilities

Validate entry database designs
Report metrics and data trends on projects
Identify data conflicts and issues on projects
Work with personnel from global research sites to resolve data conflicts
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
Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout
Comprehensive training program that provides resources and knowledge to monitor sites independently
Travel to non-local, national study sites 60-80% of the time
Communicate with medical staff and clinical research physicians on site
Utilize skills in development areas including data warehousing, business intelligence, and databases (Snowflake, ANSI SQL, SQL Server, T-SQL)
Support programming/software development using Extract, Transform, and Load (ETL) and Extract, Load and Transform (ELT) tools, (dbt, Azure Data Factory, SSIS)
Design, develop, enhance and support business intelligence systems primarily using Microsoft Power BI
Implement various recruitment strategies for clinical research studies
Work with the sites, CTM and Clinical Research Associate to discuss recruitment strategies and enrollment targets
Develop recruitment plans and ideas for new and on-going studies
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
Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial
Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards)
Build software applications and features in an Agile environment by following our software development lifecycle (SDLC) process
Develop applications in a hybrid and cloud native setting utilizing development skills that include object-oriented programming (C#), databases (SQL), Entity Framework (EF), Angular, and web applications (ASP.NET)
Participate in requirements gathering, design, development, testing, release, and support of applications