Jobs Career Advice Post Job
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Aug 6, 2025
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential ...
    Read more about this company

     

    Medical Advisor- Infectious Diseases and Vaccines, Home-Based

    Job Description

    Job Overview

    • Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects.
    • Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.

    Essential Functions

    • Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on assigned projects.
    • Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
    • May contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs).
    • May provide therapeutic area/indication training for the project clinical team.
    • Attends and may present at Investigator Meetings.
    • Performs review and clarification of trial-related Adverse Events (AEs).
    • May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
    • May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
    • May perform medical review of adverse event coding.
    • Performs review of the Clinical Study Report (CSR) and patient narratives.
    • Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
    • Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.

    Qualifications

    • Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
    • Board Certified.
    • Typically requires 3 - 5 years of prior relevant experience in general clinical medicine including experience in the requested applicable medical specialty area or equivalent combination of education, training, and experience.
    • Current knowledge of medical, scientific, and clinical landscape in applicable therapeutic area.
    • Good communication, presentation, and interpersonal skills, including good command of English language (both written and spoken).
    • Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
    • Attention to details, flexibility, and ability to provide advice on multiple assignments.
    • Current or prior license to practice medicine.
    • Clinical experience in the requested medical specialty.

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to IQVIA on jobs.iqvia.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at IQVIA Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
Send your application through

GmailGmail YahoomailYahoomail