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Clinical Research Coordinator To Home-Based Cra (Clinical Research Associate)

1+ years
$70,000 – $160,000
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 CRA (Clinical Research Associate)

Location: Phoenix, Arizona, United States
Job Category: Clinical Research Associate
Job ID: 10809


Job Summary

Medpace, a global full-service Clinical Research Organization (CRO), is seeking experienced Clinical Research Coordinators (CRCs) to advance into home-based Clinical Research Associate (CRA) roles. This position is ideal for professionals with at least one year of CRC experience who are looking to expand their career in clinical research and gain hands-on CRA experience.

Through Medpace’s PACE® Training Program, candidates receive customized, accelerated training to become fully functional CRAs. The role provides the flexibility to work from home while enjoying competitive compensation, travel bonuses, and professional growth opportunities.


Key Benefits & Incentives

  • Competitive travel bonus for site visits

  • Equity/Stock Option program for high-performing CRAs

  • Training completion and retention bonuses

  • Annual merit increases and 401(k) matching

  • Flexible home-based work schedule

  • Home office furniture allowance, laptop, mobile phone with internet hotspot

  • Retain airline and hotel reward points for travel

  • Access to in-house travel agents, airline club membership, and TSA pre-check

  • Career advancement opportunities: Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager

  • Comprehensive CRA training program (PACE®)

  • Ongoing therapeutic and regulatory training led by Medpace in-house physicians

  • Collaboration with international teams of CRAs

  • Full administrative support for all CRA levels


Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites per approved protocol

  • Communicate with site staff, including coordinators, clinical research physicians, and supporting personnel

  • Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff

  • Ensure accurate medical record and source documentation, reporting discrepancies and protocol deviations per SOPs, GCP, and regulatory standards

  • Perform on-site and remote monitoring using a risk-based monitoring approach, including centralized data review to identify deviations and implement corrective actions

  • Confirm subject eligibility and adherence to the study protocol

  • Manage regulatory documents and investigational product accountability

  • Review adverse events, serious adverse events, and concomitant medications to ensure accurate and compliant reporting

  • Assess patient recruitment and retention at sites and provide recommendations for improvement

  • Prepare monitoring reports and follow-up communications summarizing findings, deviations, and corrective actions


Qualifications & Experience Required

  • Minimum Bachelor’s degree in Health Sciences, Life Sciences, or related field

  • 1+ year experience as a Clinical Research Coordinator (CRC) or equivalent

  • Ability to travel 60–70% nationwide, with some visits conducted remotely

  • Valid driver’s license and ability to travel to monitoring sites

  • Proficient in Microsoft Office Suite

  • Strong communication, presentation, and organizational skills

  • Detail-oriented with excellent time management


Compensation

  • Target salary range: $70,000 – $160,000, depending on experience and qualifications

  • Comprehensive benefits package: medical, dental, vision, 401(k), PTO, sick days, paid holidays, work-from-home flexibility, short-term and long-term disability, life and AD&D insurance, health savings and flexible spending accounts, and pet insurance


About Medpace

Medpace is a full-service CRO providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with 5,000+ employees across 40+ countries, Medpace leverages regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace?

  • Flexible home-based work environment

  • Competitive PTO and benefits

  • Structured career growth and professional development paths

  • Employee wellness initiatives and recognition programs

  • Discounts at local businesses

  • Award-winning workplace: Top Workplace 2024 (Cincinnati Enquirer), Forbes recognition 2021–2024, and CRO Leadership Awards


Next Steps

Qualified applicants will be reviewed by Medpace’s recruitment team. Shortlisted candidates will be contacted with details for the next steps in the hiring process.