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Clinical Research Coordinator To Home-Based Clinical Research Associate (Cra) – Phoenix, Arizona

1 years
Not Disclosed
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Clinical Research Coordinator to Home-Based Clinical Research Associate (CRA) – Phoenix, Arizona

Location: United States – Phoenix, Arizona
Category: Clinical Research / Clinical Operations
Job Type: Full-Time, Remote-Eligible


Job Overview

Medpace, a leading global full-service Clinical Research Organization (CRO), is seeking experienced Clinical Research Coordinators (CRCs) to transition into Clinical Research Associate (CRA) roles. This home-based opportunity is ideal for clinical research professionals with at least one year of CRC experience, offering a structured pathway to becoming a fully functional CRA through our PACE® Training Program.

As a CRA at Medpace, you will play a critical role in the monitoring and oversight of clinical trials across the United States, ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.

This position combines remote work flexibility with nationwide travel opportunities, competitive compensation, and comprehensive professional development.


Key Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at investigational sites in compliance with approved protocols.

  • Collaborate effectively with medical site staff, including coordinators, physicians, and support personnel.

  • Verify investigator qualifications, site resources, laboratory capabilities, and staff training.

  • Review medical records and research source documentation against case report forms, ensuring accurate data capture and adherence to documentation standards.

  • Perform on-site and remote monitoring using a risk-based monitoring approach through Medpace’s integrated Clinical Trial Management System.

  • Ensure investigators enroll only eligible subjects and comply with regulatory requirements.

  • Conduct regulatory document review and oversight of investigational product accountability.

  • Assess site recruitment and retention strategies and provide recommendations to improve performance.

  • Prepare monitoring reports, highlighting deviations, deficiencies, and recommended corrective actions.


Qualifications & Experience Required

  • Education: Minimum Bachelor’s degree in a health-related or life sciences field.

  • Experience: At least 1 year of Clinical Research Coordinator (CRC) experience in a clinical trial setting.

  • Ability to travel 60–70% nationally (some visits may be conducted remotely).

  • Valid driver’s license with the ability to travel to monitoring sites.

  • Proficiency in Microsoft Office Suite.

  • Strong communication, presentation, and organizational skills.

  • Detail-oriented with excellent time management skills.

Preferred Qualifications:

  • Familiarity with global clinical trial operations and GCP compliance.

  • Experience with data management systems or electronic trial documentation.


What We Offer

  • Competitive base salary with travel bonuses and performance incentives.

  • Equity/stock option program.

  • PACE® CRA training program with ongoing therapeutic training by in-house medical experts.

  • Flexible home-based work environment and work hours.

  • Home office setup support (laptop, mobile phone with hotspot, furniture allowance).

  • Retention, training completion, and merit-based bonuses.

  • 401K matching and comprehensive benefits package.

  • Opportunities for career advancement, including Lead CRA, CRA Manager, Clinical Trial Manager, and Training & Development leadership roles.

  • Access to international CRA teams and collaborative global trial projects.


About Medpace

Medpace is a full-service, global CRO providing Phase I–IV clinical development services across biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries. We leverage scientific expertise to accelerate the development of safe and effective therapeutics in oncology, cardiology, metabolic disease, CNS disorders, anti-viral, and anti-infective research.


Why Join Medpace?

  • Work that directly impacts patient lives globally.

  • Flexible work environment with modern, eco-friendly support.

  • Competitive PTO starting at 20+ days and wellness initiatives.

  • Structured career growth paths and professional development opportunities.

  • Employee recognition programs, local business discounts, and community engagement.

  • Awarded Top Workplace 2024 (Cincinnati Enquirer) and recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).


Application Process

Qualified candidates will be reviewed by a Medpace recruitment team. Selected applicants will be contacted with details regarding the next steps in the hiring process.

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