PharmiWeb.jobs: Global Life Science Jobs

Advanced Degrees Virtual Event: June 27th

No longer accepting applications

Calling all candidates with Advanced Degrees! Join Medpace virtually on June 27th, 2024 to learn about our available positions in Clinical Research.

If interested, please fill out an application below.

Medpace will be hosting a Virtual Information Session regarding opportunities for Advanced Degree candidates who are interested in working at the Cincinnati, Ohio and Dallas, TX offices.

WHEN: Thursday, June 27th at 12:00pm ET.

  • More details regarding the format of this virtual event will be provided should you be selected to attend.

Responsibilities

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

Associate Clincial Trial Manager

  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
  • Compile and maintain project-specific status reports within the clinical trial management system;
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors;

Clinical Research Associate (CRA)

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
  • 60-80% travel to non-local, nationwide clinical study sites

Clinical Data Coordinator

  • Identify inconsistencies and discrepancies within data for project(s);
  • Work with global research site personnel to resolve data discrepancies;
  • Reconcile data across multiple sources; and
  • Create and maintain study design documents among other documentation for project(s).

Feasibility Coordinator

  • Prepare feasibility strategy
  • Summarize research across multiple sources
  • Coordinate country & site outreach; and
  • Calculate projected enrollment

Informatics Analyst

  • Query data to inform study design
  • Architect structured databases
  • Create and customize data visualizations; and
  • Automate data processing programs

Medical Writer

  • Coordinate the development of clinical study protocols and study reports with cross-functional internal and external teams including physicians, biostaticians, and clinical trial managers
  • Provide strong customer service to sponsors by delivering high quality documents within estabilished timelines.

Project Coordinator (CRO)

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

Qualifications

  • Advanced Degree in life science (Masters, PhD, Post Doc experience) - Minumum of Bachelor's degree is required for all positions;
  • 3.0 GPA or higher;
  • Willing to work office based in Cincinnati

Medpace 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 more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Today

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

  • Cincinnati Campus Overview
  • Hybrid work-from-home options (dependent upon position and level)
  • Competitive PTO packages, starting at 20+ days
  • Flexible work hours
  • Discounted tuition for UC online programs
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Competitive compensation and benefits package
  • Structured career paths with opportunities for professional growth
  • Partnership and discount with onsite childcare
  • Discounts on local sports games, local fitness gyms and attractions
    • Official Sponsor of FC Cincinnati
  • Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants
Awards

  • Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets
  • Seniority level

    Entry level
  • Employment type

    Full-time
  • Job function

    Management and Manufacturing
  • Industries

    Staffing and Recruiting

Referrals increase your chances of interviewing at PharmiWeb.jobs: Global Life Science Jobs by 2x

See who you know

Get notified about new Event Specialist jobs in Cincinnati, OH.

Sign in to create job alert

Similar jobs

People also viewed

Looking for a job?

Visit the Career Advice Hub to see tips on interviewing and resume writing.

View Career Advice Hub