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

1+ years
$70,000 - $160,000
10 Dec. 6, 2024
Job Description
Job Type: 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

The Clinical Research Coordinator to Home-Based CRA position at Medpace in Los Angeles offers an exciting opportunity for professionals with at least one year of Clinical Research Coordinator experience to transition into a Clinical Research Associate (CRA) role. Through Medpace's PACE® Training Program, you will receive the necessary training to become a fully functional CRA, with the added benefit of working remotely and earning travel bonuses.

Responsibilities:

  • Site Visits: Conduct qualification, initiation, monitoring, and closeout visits to ensure compliance with approved protocols.

  • Communication: Collaborate with site staff, including coordinators and physicians, to ensure proper implementation of clinical trials.

  • Verification: Ensure that investigators meet qualifications and that resources, such as equipment and staff, are adequate for trial needs. Verify research documentation and ensure compliance with good documentation practices.

  • Risk-Based Monitoring: Conduct both on-site and remote monitoring to identify and address site deviations and deficiencies using a risk-based approach.

  • Regulatory Compliance: Review regulatory documents, manage adverse event reporting, and ensure investigational products are properly tracked.

  • Recruitment & Retention: Evaluate patient recruitment and retention at research sites and provide recommendations for improvement.

  • Monitoring Reports: Complete monitoring reports, including summaries of findings, deviations, and recommended corrective actions.

Qualifications:

  • Education: A Bachelor's degree in a health or science-related field is required.

  • Experience: At least one year as a Clinical Research Coordinator.

  • Travel: Ability to travel 60-70% to sites nationwide, with some visits potentially being remote.

  • Skills: Proficiency in Microsoft Office, strong communication skills, and the ability to manage time effectively.

Compensation & Benefits:

  • Salary Range: $70,000 - $160,000, based on experience.

  • Perks:

    • Competitive PTO packages (20+ days)

    • Medical, dental, and vision benefits

    • 401(k) matching

    • Work-from-home flexibility

    • Paid holidays, sick days, and short/long-term disability coverage

    • Health and flexible savings accounts, life insurance, and pet insurance

Why Medpace?:

Medpace is a globally recognized full-service clinical contract research organization (CRO) committed to accelerating the global development of medical therapeutics. It has been ranked as a top workplace and recognized for its leadership and success in the industry.

Medpace offers a dynamic work environment with opportunities for career growth, flexible work arrangements, and a competitive compensation package.