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

1+ years
Not Disclosed
10 March 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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

Location: Cincinnati, Ohio
Department: Clinical Research Associate
Job ID: 10814
Employment Type: Full-Time (Remote)

Job Summary:

Medpace is growing rapidly and seeking experienced Clinical Research Associates (CRAs) to join our expanding team. As an innovative, mid-sized CRO, we focus on full-service project work and provide a customized, fast-tracked onboarding process through our Fast PACE® Training Program.

What We Offer:

  • Competitive travel bonus.
  • Equity/Stock Option program for high-performing CRAs.
  • Annual merit increases.
  • 401K matching.
  • Remote work flexibility with home office setup allowance.
  • Flexible work hours within the week.
  • Airline and hotel reward points retention.
  • Company-sponsored TSA PreCheck and airline club memberships.
  • Opportunities for leadership and career advancement (Lead CRA, CRA Manager, Clinical Trial Manager, etc.).
  • Ongoing therapeutic training by in-house physicians.
  • Dedicated administrative support for all levels of CRAs.
  • Work with an international team of CRAs.
  • Other industry-leading benefits unmatched by other CROs.

Responsibilities:

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites.
  • Communicate with site staff, including coordinators, clinical research physicians, and investigators.
  • Verify investigator qualifications, training, and resources.
  • Ensure compliance with protocols, GCP, and regulatory requirements.
  • Conduct on-site and remote monitoring with risk-based approaches.
  • Review and verify regulatory documents, adverse events, and investigational product accountability.
  • Assess and improve patient recruitment and retention strategies.
  • Complete monitoring reports summarizing findings, deviations, and corrective actions.

Qualifications:

  • Minimum 1 year of Clinical Research Associate experience.
  • Bachelor’s degree in Health Sciences, Life Sciences, or a related field.
  • Ability to travel 60-70% nationwide.
  • Proficiency in Microsoft Office.
  • Strong communication and presentation skills.
  • Detail-oriented with excellent time management skills.

#LI-Remote

Why Medpace?

For over 30 years, Medpace has been at the forefront of clinical research innovation, helping develop life-changing treatments across multiple therapeutic areas.

Cincinnati Perks:

  • Flexible work environment.
  • Competitive PTO (starting at 20+ days).
  • Comprehensive benefits package.
  • Company-sponsored appreciation events.
  • Wellness programs and on-site fitness center.
  • Tuition discounts for UC online programs.
  • Structured career advancement opportunities.

Awards & Recognition:

  • Top Workplace 2024 – The Cincinnati Enquirer.
  • Forbes – One of America’s Most Successful Midsize Companies (2021-2024).
  • CRO Leadership Awards for expertise, quality, and reliability.

Next Steps:

A Medpace team member will review your application, and if selected, you will be contacted for the next steps.

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