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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 Remote 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: San Francisco, California (Remote / Home-Based)
Job Category: Clinical Research Associate
Job ID: 10810


Job Summary

Medpace, a leading full-service Clinical Research Organization (CRO), is seeking experienced Clinical Research Coordinators (CRC) to transition into Clinical Research Associate (CRA) roles. This home-based opportunity allows clinical research professionals to advance their careers while participating in innovative Phase I–IV clinical trials across multiple therapeutic areas.

Through Medpace’s PACE® Training Program, candidates will receive personalized onboarding and training, equipping them to operate independently as a CRA while benefiting from a flexible, remote work structure. Competitive compensation, travel bonuses, and equity programs are available for high-performing CRAs.


Key Benefits & Opportunities

  • Competitive travel bonus for on-site visits

  • Equity/Stock Option Program for high performers

  • Annual merit increases and 401(k) matching

  • Flexible home-based work with adaptable scheduling

  • Home office setup support: laptop, mobile phone, hotspot, and furniture allowance

  • Travel reimbursements, airline reward points, hotel loyalty points, TSA pre-check

  • Career growth: Lead CRA, CRA Manager, Clinical Trial Manager, Training & Development Manager

  • Customized PACE® CRA training program based on prior experience, therapeutic expertise, and career goals

  • User-friendly CTMS platform for electronic submission and monitoring report approvals

  • Continuous therapeutic and regulatory training by in-house medical experts

  • Administrative support for all CRA levels

  • Collaboration with an international CRA team


Primary Responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits in compliance with protocols and GCP standards

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

  • Verify investigator qualifications, site resources, laboratories, and equipment

  • Ensure accurate source documentation and case report form data, reporting deviations per SOPs, GCP, and regulatory requirements

  • Perform on-site and remote monitoring using a risk-based approach via CTMS

  • Monitor regulatory documentation, investigational product accountability, and adverse event reporting

  • Evaluate site patient recruitment and retention and provide recommendations for improvement

  • Complete monitoring reports with summaries of deviations, deficiencies, and recommended corrective actions


Required Experience & Qualifications

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

  • Bachelor’s degree in health sciences, life sciences, or related field

  • Ability to travel 60–70% nationwide; remote monitoring options available

  • Valid driver’s license for site visits

  • Proficient in Microsoft Office Suite

  • Strong communication, presentation, and organizational skills

  • Detail-oriented with excellent time management and problem-solving abilities


Compensation & Benefits

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

  • Medical, dental, vision, 401(k), PTO starting at 20+ days, sick leave, paid holidays

  • Work-from-home flexibility, short- and long-term disability, HSA/FSA accounts, life and AD&D insurance

  • Pet insurance, career growth programs, and leadership development opportunities


Why Medpace?

  • Join a globally recognized, mid-sized CRO driving clinical innovation across therapeutic areas

  • Work on cutting-edge clinical trials with home-based flexibility

  • Access to ongoing training programs and international collaboration

  • Strong career progression with clear leadership pathways


Awards & Recognition

  • Named a Top Workplace in 2024 by The Cincinnati Enquirer

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)

  • Continually awarded CRO Leadership Awards by Life Science Leader for expertise, quality, and reliability


Next Steps

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