Qureos Mentor

Medpace

<div>Job Summary :
<div>
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Engineer to join our Information Technology team. This position will work on a team to accomplish tasks and projects that are instrumental to the company&rsquo;s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.</div>
Responsibilities :
<ul><li>Utilize skills in development areas including data warehousing, business intelligence, and databases (Snowflake, ANSI SQL, SQL Server, T-SQL);</li><li>
Support programming/software development using Extract, Transform, and Load (ETL) and Extract, Load and Transform (ELT) tools, (dbt, Azure Data Factory, SSIS);</li><li>
Design, develop, enhance and support business intelligence systems primarily using Microsoft Power BI;</li><li>
Collect, analyze and document user requirements;</li><li>
Participate in software validation process through development, review, and/or execution of test plan/cases/scripts;</li><li>
Create software applications by following software development lifecycle process, which includes requirements gathering, design, development, testing, release, and maintenance;</li><li>
Communicate with team members regarding projects, development, tools, and procedures; and</li><li>
Provide end-user support including setup, installation, and maintenance for applications</li></ul>
Qualifications :
<ul><li>Bachelor's Degree in Computer Science, Data Science, or a related field;</li><li>
3+ years of experience in Data Engineering;</li><li>
Knowledge of developing dimensional data models and awareness of the advantages and limitations of Star Schema and Snowflake schema designs;</li><li>
Solid ETL development, reporting knowledge based off intricate understanding of business process and measures;</li><li>
Knowledge of Snowflake cloud data warehouse, Fivetran data integration and dbt transformations is preferred;</li><li>
Knowledge of Python is preferred;</li><li>
Knowledge of REST API;</li><li>
Basic knowledge of SQL Server databases is required;</li><li>
Knowledge of C#, Azure development is a bonus; and</li><li>
Excellent analytical, written and oral communication skills.</li></ul>
Medpace Overview :
<div>
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 6,000 people across 40+ countries.</div>
Why Medpace? :
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div><br>
The work we&rsquo;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.</div><div></div><p><b><br>
Medpace Perks</b></p><ul><li>
Flexible work environment</li><li>
Competitive compensation and benefits package</li><li>
Competitive PTO packages</li><li>
Structured career paths with opportunities for professional growth</li><li>
Company-sponsored employee appreciation events
</li><li>Employee health and wellness initiatives</li></ul><div><b>
Awards</b></div><ul><li>
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul><div></div><div><b><br>
What to Expect Next</b></div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Data Engineer

<div>Job Summary :
<div>
Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in London. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in the UK. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel.</div><div></div><div><br>
If you want an exciting career within a company that excels in delivering innovative research and development of cutting edge drugs, where you can grow your potential, then this is the opportunity for you.</div>
Responsibilities :
<ul><li>Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;</li><li>
Develop effective plans for site contact and follow-up;</li><li>
Support management in expediting feasibility, site selection and study start-up; and</li><li>
May be responsible for other projects and responsibilities as assigned.</li><li>
Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country;</li><li>
Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up;</li><li>
Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention;</li><li>
Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors</li><li>
Conducting regular performance reviews for sites participating to our studies, ensuring quality study delivery</li><li>
Serve as an escalation point for site related issues throughout the life cycle of a study</li><li>
Provide ongoing support of sites, including identifying and discussing future new business;</li><li>
Develop effective plans for site contacts, troubleshooting, and follow-up;</li><li>
Develop an intelligence database with site and country intelligence</li><li>
Support Management with process improvement initiatives regarding feasibility activities</li><li>
Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information; and</li><li>
May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.</li></ul>
Qualifications :
<ul><li>Minimum a Bachelor of Science in health-related field;</li><li>
Minimum 1 years' site and clinical trials experience (more experience for the more senior positions required);</li><li>
CRA experience is an asset;</li><li>
Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;</li><li>
Knowledge of medical terminology and clinical patient management preferred;</li><li>
Fluency in English;</li><li>
Demonstrated organizational and prioritization skills;</li><li>
Excellent oral and written communication skills; and</li><li>
Proficient knowledge of Microsoft Office applications.</li></ul><div></div><div><b><br>
We kindly ask to send applications in English.</b></div><div></div><div><b><br>
WHY MEDPACE?</b></div><div>
At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.</div><div></div><div><b><br>
WHAT TO EXPECT NEXT</b></div><div>
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an initial phone interview.</div><br>
<div></div>
Medpace Overview :
<div>
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 6,000 people across 40+ countries.</div>
Why Medpace? :
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div><br>
The work we&rsquo;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.</div><div></div><p><b><br>
Medpace Perks</b></p><ul><li>
Flexible work environment</li><li>
Competitive compensation and benefits package</li><li>
Competitive PTO packages</li><li>
Structured career paths with opportunities for professional growth</li><li>
Company-sponsored employee appreciation events
</li><li>Employee health and wellness initiatives</li></ul><div><b>
Awards</b></div><ul><li>
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul><div></div><div><b><br>
What to Expect Next</b></div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Data Engineer (AI) - Cincinnati

<div>Job Summary:
<div><b>
Join our team in Cincinnati!</b> Medpace is a contract research organization (CRO) with a mission to advance new and better medical treatments that improve lives. As our creative services expand, we are seeking recent graduates and experienced designers who can apply their layout and design skills to diverse projects.</div><div></div><div><br>
As a <b>Design Coordinator</b>, you will be an integral member of the <b>Information Design team</b>&mdash;a group of writers, designers, technical communicators, and other creative individuals who are passionate about improving lives. We provide creative guidance and develop compelling content, branding, documents, and trainings for a wide audience.</div>
Responsibilities :
<ul><li>Design and format clinical study materials (e.g., worksheets, informational cards, questionnaires) for patients, caregivers, research site staff, and physicians</li><li>
Incorporate amendments and translations into existing documents using Adobe InDesign, Adobe Illustrator, and Microsoft Word;</li><li>
Manage translations to deliver high-quality materials around the globe
</li><li>Keep study teams informed by tracking study materials for regulatory submission<br>
Review study materials to ensure they reflect source documentation</li></ul><div>
Skills/Characteristics</div><ul><li>
Enjoy applying your skills in design, writing, editing, communication, and organization to diverse projects</li><li>
Embrace new projects and prioritize requests in a fast-paced, collaborative environment</li><li>
Desire to become an expert in how translations affect design and layout</li></ul>
Qualifications :
<ul><li>Willing to work fully office-based;</li><li>
Bachelor&rsquo;s degree (design-related degree or design experience preferred);</li><li>
Significant experience with file structure and file management;</li><li>
Advanced knowledge of Adobe InDesign and Adobe Illustrator; and</li><li>
Advanced knowledge of Microsoft Word, including applying styles and using templates.</li></ul>
Medpace Overview :
<div>
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 6,000 people across 40+ countries.</div>
Why Medpace?:
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div><br>
The work we&rsquo;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.</div><div></div><div><b><br>
Cincinnati Perks</b></div><ul><li>
Cincinnati Campus Overview</li><li>
Competitive PTO packages, starting at 20+ days</li><li>
Competitive compensation and benefits package</li><li>
Company-sponsored employee appreciation events</li><li>
Employee health and wellness initiatives</li><li>
Community involvement with local nonprofit organizations</li><li>
Discounts on local sports games, fitness gyms and attractions</li><li>
Modern, ecofriendly campus with an on-site fitness center</li><li>
Structured career paths with opportunities for professional growth</li><li>
Discounted tuition for UC online programs</li></ul><div><b>
Awards</b></div><ul><li><div>
Named a Top Workplace in 2024 by The Cincinnati Enquirer</div></li><li>
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul><div><br>
</div><div></div><div><b>What to Expect Next</b></div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Production Artist

<div>
 Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you are seeking an
 <strong>
  exciting, entry-level position
 </strong>
 where you can build a foundation in the
 <strong>
  clinical research industry
 </strong>
 and
 <strong>
  develop/grow your career
 </strong>
 through our robust training program, then this is the opportunity for you.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   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;
  </li>
  <li>
   Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  </li>
  <li>
   Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards); and
  </li>
  <li>
   Maintain timelines for study start-up through internal team collaboration.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  SITE ACTIVATION &amp; MAINTENANCE (SAM) TRAINING PROGRAM
  <br/>
  <br/>
 </strong>
 Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM Training Program embraces evidence based learning &amp; development models to advance professional learning and employee performance. In the program, you will&hellip;
 <br/>
 <br/>
 <ul>
  <li>
   Complete independent learning modules, interactive exercises, and team workshops through the core curriculum;
  </li>
  <li>
   Gain exposure to real-world tasks through a robust mentoring program; and
  </li>
  <li>
   Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree is required (Life Sciences field preferred);
  </li>
  <li>
   Some experience in an office setting is preferred;
  </li>
  <li>
   Excellent organizational and prioritization skills;
  </li>
  <li>
   Knowledge of Microsoft Office; and
  </li>
  <li>
   Great attention to detail and excellent oral and written communication skills.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Travel:
 </strong>
 None
 <br/>
 <br/>
 <strong>
  Medpace Overview
  <br/>
  <br/>
 </strong>
 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 6,000 people across 40+ countries.
 <br/>
 <br/>
 <strong>
  Why Medpace?
  <br/>
  <br/>
 </strong>
 People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
 <br/>
 <br/>
 The work we&rsquo;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.
 <br/>
 <br/>
 <strong>
  Cincinnati Perks
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Cincinnati Campus Overview
  </li>
  <li>
   Flexible work environment
  </li>
  <li>
   Competitive PTO packages, starting at 20+ days
  </li>
  <li>
   Competitive compensation and benefits package
  </li>
  <li>
   Company-sponsored employee appreciation events
  </li>
  <li>
   Employee health and wellness initiatives
  </li>
  <li>
   Community involvement with local nonprofit organizations
  </li>
  <li>
   Discounts on local sports games, fitness gyms and attractions
  </li>
  <li>
   Modern, ecofriendly campus with an on-site fitness center
  </li>
  <li>
   Structured career paths with opportunities for professional growth
  </li>
  <li>
   Discounted tuition for UC online programs
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Awards
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Named a Top Workplace in 2024 by The Cincinnati Enquirer
  </li>
  <li>
   Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  </li>
  <li>
   Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What To Expect Next
  <br/>
  <br/>
 </strong>
 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
</div>


Entry-Level Study Start-Up Coordinator

<div>Responsibilities :
<ul><li>Serve as Subject Matter Expert (SME) for applications that support the Accounting department, as well as related processes;</li><li>
Serve as liaison between the Accounting application users and IT project teams to facilitate efficient development and support;</li><li>
Participate in the software validation process through development, review and/or execution of testing;</li><li>
Assess current state, identify customer requirements, and define future state and/or business solution based on customer needs;</li><li>
Research, gather and synthesize information;</li><li>
Provide end-user support including identifying application improvements, researching and triaging issues, and defect tracking for Accounting systems.</li></ul>
Qualifications :
<ul><li>Bachelor degree in Management Information Systems (MIS), Accounting or related field;</li><li>
2-3 years of Business Analyst experience;</li><li>
SQL experience preferred;</li><li>
High degree of professionalism;</li><li>
Works well in a team environment, focused on career growth and development</li></ul>
Medpace Overview :
<div>
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.</div>
Why Medpace?:
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div><br>
The work we&rsquo;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.</div><div></div><div><b><br>
Cincinnati Perks</b></div><ul><li>
Cincinnati Campus Overview</li><li>
Flexible work environment</li><li>
Competitive compensation</li><li>
Company-sponsored employee appreciation events</li><li>
Employee health and wellness initiatives</li><li>
Community involvement with local nonprofit organizations</li><li>
Discounts on local sports games, fitness gyms and attractions</li><li>
Modern, ecofriendly campus with an on-site fitness center</li></ul><div></div><div><b><br>
What to Expect Next</b></div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Business Systems Analyst- Accounting

<div>
 <strong>
  Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
  <br/>
  <br/>
 </strong>
 This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our
 <em>
  PACE&reg;
 </em>
 Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary.
 <br/>
 <br/>
 <strong>
  WE OFFER THE FOLLOWING
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive travel bonus;
  </li>
  <li>
   Equity/Stock Option program;
  </li>
  <li>
   Training completion and retention bonus
  </li>
  <li>
   Annual merit increases;
  </li>
  <li>
   401K matching;
  </li>
  <li>
   The opportunity to work from home;
  </li>
  <li>
   Flexible work hours across days within a week;
  </li>
  <li>
   Retain airline reward miles and hotel reward points;
  </li>
  <li>
   Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
  </li>
  <li>
   In-house travel agents, reimbursement for airline club, and TSA pre-check;
  </li>
  <li>
   Opportunity for leadership positions &ndash; Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
  </li>
  <li>
   CRA training program (PACE&reg;);
  </li>
  <li>
   Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
  </li>
  <li>
   In-house administrative support for all levels of CRAs; and
  </li>
  <li>
   Opportunities to work with international team of CRAs.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  </li>
  <li>
   Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
  </li>
  <li>
   Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  </li>
  <li>
   Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
  </li>
  <li>
   On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;
  </li>
  <li>
   Verification that the investigator is enrolling only eligible subjects;
  </li>
  <li>
   Regulatory document review;
  </li>
  <li>
   Medical device and/or investigational product/drug accountability and inventory;
  </li>
  <li>
   Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
  </li>
  <li>
   Assess the clinical research site&rsquo;s patient recruitment and retention success and offering suggestions for improvement; and
  </li>
  <li>
   Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Must have a minimum of a Bachelor&rsquo;s degree in a health or science related field;
  </li>
  <li>
   Experience as a Clinical Research Coordinator (minimum 1 year);
  </li>
  <li>
   Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
  </li>
  <li>
   Must maintain a valid driver&rsquo;s license and the ability to drive to monitoring sites;
  </li>
  <li>
   Proficient knowledge of Microsoft&reg; Office;
  </li>
  <li>
   Strong communication and presentation skills; and
  </li>
  <li>
   Must be detail-oriented and efficient in time management.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <br/>
  <br/>
 </strong>
 <strong>
  Medpace Overview
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  Why Medpace?
  <br/>
  <br/>
 </strong>
 People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
 <br/>
 <br/>
 The work we&rsquo;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.
 <br/>
 <br/>
 <strong>
  Medpace Perks
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Flexible work environment
  </li>
  <li>
   Competitive PTO packages &ndash; starting at 20+ days
  </li>
  <li>
   Company-sponsored employee appreciation events
  </li>
  <li>
   Employee health and wellness initiatives
  </li>
  <li>
   Competitive compensation and benefits package
  </li>
  <li>
   Structured career paths with opportunities for professional growth
  </li>
  <li>
   Discounts for local businesses
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Awards
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Named a Top Workplace in 2024 by The Cincinnati Enquirer
  </li>
  <li>
   Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  </li>
  <li>
   Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What To Expect Next
  <br/>
  <br/>
 </strong>
 A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
 <br/>
 <br/>
</div>


Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Join Medpace and explore 7   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.