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Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity

November 20, 2025

Experienced Clinical Research Associate (CRA) - join our growing team!Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work.Through our fast PACE® Training Program, you will receive customized, expedited training, and efficient onboarding to familiarize you with Medpace systems. WE OFFER THE FOLLOWING:<ul><li>Competitive travel bonus;</li><li>Equity/Stock Option program for high performing CRAs;</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/career advancement – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager;</li><li>Customized Fast PACE® training program based on your experience, therapeutic background, and interest;</li><li>User friendly CTMS with electronic submission and approval of monitoring visit reports;</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;</li><li>Opportunities to work with international team of CRAs; and</li><li>Many additional perks unmatched by other CROs!</li></ul> Responsibilities <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’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.</li></ul> Qualifications <ul><li>Clinical Research Associate Experience (minimum 1 year);</li><li>Ability to travel 60-70% to locations nationwide is required;</li><li>Must have a minimum of a bachelor’s degree in a health or science related field;</li><li>Proficient knowledge of Microsoft® Office;</li><li>Strong communication and presentation skills; and</li><li>Must be detail-oriented and efficient in time management.</li></ul> #LI-Remote 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 Us 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<ul><li><a href="https://medpace.icims.com/icims2/servlet/icims2?module=AppInert&action=download&id=636074&hashed=-704132284" target="_blank" rel="noopener">Cincinnati Campus Overview</a></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</li></ul>Awards<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</li></ul><img src="https://medpace.icims.com/icims2/servlet/icims2?module=AppInert&action=download&id=1012864&hashed=-1853293896" alt="TWP 2024" width="75" height="139"> <img src="https://medpace.icims.com/icims2/servlet/icims2?module=AppInert&action=download&id=1020742&hashed=-276143562" alt="CRO2024" width="340" height="116"> What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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DISCLAIMER

Get Hired Faster With COMPANY_NAME!

1: COMPANY_NAME Smart Tools and Direct Employer Connections Help Speed Up Your Hiring Process

2: With Better Matches, Real-time Job Alerts, and Direct Employer Responses, COMPANY_NAME Helps Many Candidates Secure Interviews and Job Offers Within 15 to 30 Days!

3: The Type of Resume You Need to Get Priority Placement

4: Browse Full-Time, Part-Time, and Freelancing Roles With COMPANY_NAME

5: COMPANY_NAME Helps You Grow Your Career

6: The Easiest Way To Find A Job

7: Find Roles That Offer Growth, Culture & Benefits

8: Get Support With Resume, Interviews & Career Planning

9: Your Future Starts Today

10: Get Hired Within 15 to 30 Days With COMPANY_NAME

Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity

Common Interview Questions And Answers

1. HOW DO YOU PLAN YOUR DAY?

2. HOW DO YOU USE THE DIFFERENT COMMUNICATION TOOLS IN DIFFERENT SITUATIONS?

3. WHAT IS "WORKING REMOTE" REALLY FOR YOU?

4. WHAT DO YOU NEED IN YOUR PHYSICAL WORKSPACE TO SUCCEED IN YOUR WORK?

5. HOW DO YOU PROCESS INFORMATION?

6. HOW DO YOU MANAGE THE CALENDAR AND THE PROGRAM? WHICH APPLICATIONS / SYSTEM DO YOU USE?

7. HOW DO YOU ORGANIZE FILES, LINKS, AND TABS ON YOUR COMPUTER?

8. HOW TO PRIORITIZE WORK?

9. HOW DO YOU PREPARE FOR A MEETING AND PREPARE A MEETING? WHAT DO YOU SEE HAPPENING DURING THE MEETING?

10. HOW DO YOU USE TECHNOLOGY ON A DAILY BASIS, IN YOUR WORK AND FOR YOUR PLEASURE?

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