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    Principal Investigator (Md/Do) For Clinical Trials

    Barrington James
    1-6 years
    Not Disclosed
    Scottsdale
    10 Aug. 16, 2024
    Job Description
    Job Type: Full Time 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: Principal Investigator (MD/DO) for Clinical Trials – Women’s Health

    Company: Confidential Clinical Research Centre

    Location: Remote/Flexible (Must be based in or near Scottsdale, Arizona)

    About the Company:

    We are a unique and innovative clinical research organization dedicated to expanding clinical research into private clinics. Our commitment lies in delivering high-quality support to our partners and ensuring optimal outcomes for patients through advanced research methods.

    Position Overview:

    We are seeking a dedicated MD or DO to join our team as a Principal Investigator specializing in women’s health. This role is perfect for a full-time physician interested in diversifying their income and supporting patient care through clinical research.

    Key Responsibilities:

    • Maintain up-to-date Good Clinical Practice (GCP) certification.
    • Attend occasional sponsor meetings, both in-person and virtual.
    • Review patient charts, lab results, and other relevant data remotely.
    • Complete various regulatory documents as required.

    Qualifications:

    • Medical Doctor (MD) or Doctor of Osteopathic Medicine (DO) degree.
    • Active and current medical license.
    • Up-to-date GCP certification.
    • Strong organizational and communication skills.
    • Experience with clinical trials is preferred but not mandatory.

    Commitment and Flexibility:

    • Flexible time commitment that can be adjusted to fit your schedule, provided regulatory guidelines are met.
    • Number of studies managed will vary based on availability and personal preference.

    Benefits:

    • Competitive compensation based on the number of trials managed.
    • Opportunity to enhance patient care through participation in groundbreaking clinical research.
    • Flexibility to manage your time and work remotely.

    How to Apply:

    If you are a motivated physician specializing in women’s health and interested in advancing your career in clinical research, we would love to hear from you!

    Please submit your CV to: gjohnstone@barringtonjames.com or call +44 1293 778 666 for more information.

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