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

Medpace
1+ years
USD $75,000–$110,000
Phoenix, United States
15 June 24, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Research Coordinator to Home-Based Clinical Research Associate (CRA)

Company: Medpace
Job Title: Clinical Research Coordinator to Home-Based Clinical Research Associate (CRA)
Job ID: 11847
Location: Phoenix, Arizona, USA (Remote/Home-Based)

Salary: USD $75,000–$110,000 per year (Estimated) + Travel Bonus + Equity/Stock Options + Retention Bonus + Annual Merit Increases


Job Summary

Medpace is seeking experienced Clinical Research Coordinators (CRCs) who are interested in transitioning into a Clinical Research Associate (CRA) role. Through the company's PACE® Training Program, successful candidates will receive comprehensive CRA training and have the opportunity to work remotely while supporting clinical trials nationwide.

This position is ideal for CRCs with at least one year of clinical research experience who are looking to advance their careers into clinical monitoring.


What Medpace Offers

  • Competitive travel bonus program

  • Equity/Stock Option Program

  • Training completion and retention bonuses

  • Annual salary increases based on performance

  • 401(k) matching program

  • Home-based work opportunity

  • Flexible scheduling

  • Retention of airline miles and hotel reward points

  • Home office furniture allowance

  • Company-provided laptop and mobile phone with hotspot

  • In-house travel support services

  • TSA PreCheck and airline club reimbursement

  • International collaboration opportunities

  • Defined leadership and career progression pathways


PACE® CRA Training Program

The Medpace PACE® Program provides:

  • Comprehensive Clinical Research Associate training

  • Ongoing therapeutic-area education

  • Training from in-house physicians and regulatory experts

  • Practical monitoring experience

  • Administrative support throughout career development

  • Opportunities for advancement into senior leadership roles

Potential Career Progression

  • Clinical Research Associate (CRA)

  • Senior CRA

  • Lead CRA

  • CRA Manager

  • Clinical Trial Manager

  • Training & Development Manager


Key Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits

  • Perform both on-site and remote monitoring activities

  • Review source documents and verify study data accuracy

  • Ensure protocol, GCP, SOP, and regulatory compliance

  • Verify investigator qualifications and site readiness

  • Monitor patient eligibility and enrollment activities

  • Review regulatory documentation

  • Manage investigational product/device accountability

  • Review adverse events (AEs) and serious adverse events (SAEs)

  • Assess patient recruitment and retention performance

  • Identify site risks and implement corrective/preventive actions

  • Prepare monitoring reports and follow-up letters

  • Communicate effectively with investigators, coordinators, and site staff


Eligibility Criteria

Required Qualifications

  • Bachelor's degree in a Health Science, Life Science, Nursing, Pharmacy, Biotechnology, or related field

  • Minimum 1 year of Clinical Research Coordinator (CRC) experience

  • Ability to travel approximately 60–70% nationwide

  • Valid driver's license and ability to drive to monitoring sites

  • Proficiency in Microsoft Office

  • Strong communication and presentation skills

  • Excellent organizational and time-management abilities

  • Strong attention to detail


Work Environment

  • Remote/Home-Based position

  • Combination of on-site and virtual monitoring

  • Nationwide travel required

  • Flexible work schedule


Employee Benefits

  • Competitive compensation package

  • Medical, dental, and vision benefits

  • PTO starting at 20+ days annually

  • Employee wellness programs

  • Employee appreciation events

  • Professional development opportunities

  • Discounts with local businesses

  • Structured career growth pathways


About Medpace

Medpace is a global full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,000 professionals across 40+ countries and supports clinical research in oncology, cardiology, endocrinology, metabolic diseases, CNS disorders, infectious diseases, and other therapeutic areas.


Awards & Recognition

  • Top Workplace 2024 – Cincinnati Enquirer

  • Forbes America's Most Successful Midsize Companies (2021–2024)

  • Multiple CRO Leadership Awards for quality, expertise, reliability, and client satisfaction