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

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: Los Angeles, California, United States
Job Category: Clinical Research Associate
Job ID: 10811


Job Summary

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

Through Medpace’s PACE® Training Program, candidates receive customized training and onboarding to become fully functional CRAs, with the flexibility to work home-based while benefiting from a competitive salary and performance-based travel bonuses.


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 work-from-home schedule

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

  • Retain airline and hotel reward points

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

  • Leadership and career advancement opportunities: Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and more

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

  • Collaboration with an international team of CRAs

  • Comprehensive administrative support for all CRA levels


Responsibilities

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

  • Communicate effectively 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, addressing discrepancies and protocol deviations per SOPs, GCP, and regulatory requirements

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

  • Verify subject eligibility and monitor adherence to the protocol

  • Manage regulatory documents and investigational product accountability

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

  • Assess site patient recruitment and retention, providing actionable recommendations

  • Prepare monitoring reports and follow-up letters 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; some visits may be remote

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

  • Proficiency in Microsoft Office Suite

  • Strong communication, presentation, and organizational skills

  • Detail-oriented with efficient time management


Compensation

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

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


Medpace Overview

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


Why Medpace?

  • Flexible work environment with home-based opportunities

  • Competitive PTO and benefits

  • Structured career growth and professional development paths

  • Employee wellness 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 the Medpace recruitment team. Shortlisted candidates will be contacted with next steps for the hiring process.