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Medical and Scientific Reviewer
Zenith Leap Solution Pvt. Ltd
  • 5 - 10 yrs
  • Not Mentioned
  • Gorakhpur
  • Understanding of medical terminology clinical trials drug development process Exceptional communication skills including written oral interpersonal Excellent project management skills Strong scientific and medical acumen and ability to grasp complex therapeutic areas
    • Full Time
    graduate
    5 - 10 yrs
    No required
    3
    Zenith Leap Solution Pvt. Ltd
    Full Time

    Working Type : Work From Office
    Job Description :

    EVERSANA

    Job Description

    THE POSITION:
    At EVERSANA, we provide end-to-end integrated global medical information and medical affairs services
    for various life sciences companies, including pharmaceutical, biotechnology, medical device, digital
    therapeutics, and over-the-counter companies of various sizes, including industry leaders and emerging
    companies. Additionally, we provided therapeutic area support across oncology, hematology, rare
    diseases, immunology, cardiology, dermatology, urology, gastroenterology, infectious diseases,
    nephrology, neurology, pain, rheumatology, respiratory, ophthalmology, endocrinology, pulmonology,
    hepatology, consumer products, woman’s health and more.
    This position will be part of our global medical content development and medical / scientific review team.
    This role requires medical and scientific expertise, an understanding of regulations and best practices for
    promotional and non-promotional materials, high attention to detail and medical / scientific accuracy, the
    ability to analyze / translate / interpret scientific literature and data, the ability to quickly learn new
    therapeutic areas, and excellent communication skills (both verbal and written).

    ESSENTIAL DUTIES AND RESPONSIBILITIES:
    Our employees are tasked with delivering excellent business results through the efforts of their teams.
    These results are achieved by:
    ï‚· Perform scientific data fact-checking and review of promotional and non-promotional
    materials that are submitted for medical, legal, and regulatory (MLR) review meetings.
    ï‚· Ensure that data are scientifically accurate, contextually correct, editorially accurate, and are
    presented in a fair/scientifically balanced manner with minimal supervision and in a timely
    manner:
    o Ensures scientific accuracy, relevance, and completeness of data
    o Ensures claims and data are clinically and statistically relevant and presented in a
    scientifically balanced manner (not false or misleading)
    o Ensures that claims are adequately supported by data
    o Determines acceptability of references
    o Advises on whether claims are consistent with the approved label
    o Ensure that the piece is relevant and of utility for the target audience
     Ensure that information and data presented aligns and are consistent with the client’s

    Qualifications:-


    The requirements listed below are representative of the experience, education, knowledge, skill, and/or
    abilities required.
    ï‚· PharmD (or M. Pharm. or M.S. Pharm), Ph.D., BDS, MDS, or MBBS with relevant experience
    in scientific writing and/or reviewing.
    ï‚· Minimum of 2 years of experience in document QC and/or scientific writing within the life
    science and/or pharmaceutical industry.
    ï‚· Experience conducting literature searches and analysis and working with tools such as
    RightFind, PubMed, Ovid, Embase, etc.
    ï‚· Strong scientific and medical acumen and ability to grasp complex therapeutic areas (e.g.,
    rare diseases, immunology, oncology / hematology, gene therapy).
    ï‚· Understanding of medical terminology, clinical trials, and drug development process.
    ï‚· Ability to analyze and interpret scientific and medical data and translate it for different
    audiences (e.g., HCPs, payers, patients / caregivers).
    ï‚· Highly detailed orientated and excellent time management skills.
    ï‚· Exceptional communication skills including, written, oral, interpersonal, and presentation
    skills including the ability to independently interpret and summarize complex results.
    ï‚· Experience using content development and management tools and review / approval
    platforms (e.g., Veeva Vault PromoMats / MedComms).
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