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Job description
Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity
Join to apply for the Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity role at Medpace.
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‑size 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:
Competitive travel bonus
Equity/Stock Option program for high performing CRAs
Annual merit increases
401(k) matching
The opportunity to work from home
Flexible work hours across days within a week
Retain airline reward miles and hotel reward points
Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
In‑house travel agents, reimbursement for airline club, and TSA pre‑check
Opportunity for leadership positions/career advancement – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager
Customized Fast PACE® training program based on your experience, therapeutic background, and interest
User friendly CTMS with electronic submission and approval of monitoring visit reports
Ongoing therapeutic training by our in‑house physicians who are medical and regulatory experts
In‑house administrative support for all levels of CRAs
Opportunities to work with international team of CRAs
Many additional perks unmatched by other CROs
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
Communicate with the medical site staff including coordinators, clinical research physicians, and their site staff
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
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
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
Verification that the investigator is enrolling only eligible subjects
Regulatory document review
Medical device and/or investigational product/drug accountability and inventory
Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
Completion of monitoring reports and follow‑up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Qualifications
Clinical Research Associate Experience (minimum 1 year)
Ability to travel 60‑70% to locations nationwide
Must have a minimum of a bachelor’s degree in a health or science related field
Proficient knowledge of Microsoft® Office
Strong communication and presentation skills
Detail‑oriented and efficient in time management
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
Cincinnati Campus Overview
Flexible work environment
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Company‑sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with local nonprofit organizations
Discounts on local sports games, fitness gyms and attractions
Modern, eco‑friendly campus with an on‑site fitness center
Structured career paths with opportunities for professional growth
Discounted tuition for UC online programs
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
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.
Seniority level: Not applicable
Employment type: Full‑time
Job function: Research, Analyst, and Information Technology
Industries: Pharmaceutical Manufacturing
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Worksite address
cincinnati, OH, 45208, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.