Instagram
youtube
Facebook

Home-Based Experienced Cra (Clinical Research Associate)- Bonus/Equity

1-3 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Remote 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

Job Title: Home-Based Experienced Clinical Research Associate (CRA) - Bonus/Equity

Location: Cincinnati, Ohio (Home-Based with Flexible Work Options)
Job Type: Full-time


ABOUT MEDPACE

Medpace is an innovative, scientifically oriented mid-sized global contract research organization (CRO). We specialize in full-service project work and focus on accelerating the global development of safe and effective medical therapeutics. We are growing rapidly and looking for experienced Clinical Research Associates (CRAs) to join our dynamic team.


JOB SUMMARY

Medpace is seeking experienced CRAs to join our team in a home-based role. This opportunity provides competitive compensation, including equity/stock options, bonus programs, and a flexible work environment. In addition, the position offers career advancement opportunities through leadership roles and access to our Fast PACE® Training Program, designed to expedite onboarding and improve your skills in the clinical research field.


KEY RESPONSIBILITIES

Site Management & Monitoring

  • Conduct qualification, initiation, monitoring, and closeout visits at clinical research sites, ensuring compliance with the protocol.
  • Communicate regularly with site staff, including coordinators and clinical research physicians.
  • Verify investigator qualifications and ensure adequate resources, including staff, facilities, and equipment.

Documentation & Compliance

  • Review medical records and source documentation, ensuring consistency with case report forms (CRFs) and compliance with good documentation practices (GDP).
  • Identify and report any protocol deviations to the site staff and take corrective actions in line with SOPs and GCP guidelines.
  • Perform both on-site and virtual/remote monitoring, using a risk-based monitoring approach to ensure compliance and mitigate risks.

Regulatory & Safety Monitoring

  • Verify the eligibility of subjects enrolled in the trial and ensure compliance with regulatory documents and clinical trial protocols.
  • Monitor adverse events (AEs) and serious adverse events (SAEs), ensuring accurate data reporting.
  • Ensure proper accountability of investigational products and medical devices at the research sites.

Reporting & Recommendations

  • Prepare and submit monitoring reports and follow-up letters, summarizing significant findings, deviations, and recommended actions.
  • Assess and improve patient recruitment and retention strategies at the clinical sites.

QUALIFICATIONS & EXPERIENCE

Education:

  • Bachelor’s degree in a health or science-related field.

Experience:

  • Minimum of 1 year of independent CRA experience or relevant clinical research experience.

Skills & Competencies:

  • Proficient in Microsoft Office and other relevant software tools.
  • Strong communication and presentation skills.
  • Detail-oriented, with strong time management and organizational skills.
  • Ability to travel 60-70% for site visits nationwide.

COMPENSATION & BENEFITS

Salary & Benefits:

  • Competitive salary with annual merit increases.
  • Equity/Stock Option program and travel bonuses for high-performing CRAs.
  • 401K matching and comprehensive health, dental, and vision insurance.
  • Flexible work hours with the ability to work from home.

Career Development & Perks:

  • Customized Fast PACE® training program to enhance clinical research skills.
  • Leadership opportunities for career advancement (Lead CRA, CRA Manager, Clinical Trial Manager, etc.).
  • Home office furniture allowance, laptop, and mobile phone with hotspot for internet access.
  • Retain airline reward miles and hotel reward points.
  • In-house administrative support for CRAs at all levels.

AWARDS & RECOGNITION

  • Top Workplace in 2024 by The Cincinnati Enquirer.
  • Forbes: Recognized as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
  • CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility.

WHY MEDPACE?

  • People, Purpose, Passion – Join Medpace to make a meaningful difference in the world of clinical research.
  • The work we do today will improve the lives of patients living with various illnesses and diseases across all key therapeutic areas.

HOW TO APPLY

Accelerate your career by joining Medpace. Apply today to become a part of a growing team committed to improving global health and making a lasting impact.