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    Job · 13571916

    ProPharma Group logo

    Medical Information Writer

    ProPharma Group · Hyderabad · onsite · Posted 59d ago

    Undisclosed2–7 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Job Summary

    The Medical Information Writer role is responsible for writing technical responses such as letters or frequently asked questions (FAQs) to be used to answer enquiries received by Medical Information. This may involve updating existing responses or writing new standard responses. Production of other documents may be required.

    Responsibilities

    • Carrying out comprehensive and accurate literature searches in Medline, or other databases as required, for technical medical information letters or documents.
    • Preparing medical information letters and other documents using information gathered from literature searches or similar technical information. This may require condensing large amounts of technical data into concise and readable standard documents.
    • Updating existing written documents, by checking the information within them is still accurate and up to date, and adding new information identified from literature searches in the most appropriate places to ensure readability and technical flow.
    • Ensuring that all written items are accurate, readable and technically proficient and comply with ProPharma SOPs and the requirements of the client as defined in client specific Working Practices. Quality Assurance
    • Quality checking own work and checking simple documents of others within the team under guidance to ensure standards are met and maintained.
    • Maintaining awareness of, and ensuring compliance with, the legal requirements and professional guidelines associated with the provision of medical information within the pharmaceutical and healthcare industries.
    • Ensuring that the Confidentiality Statement within the Contract of Employment is adhered to at all times in respect of the data and property of ProPharma and its clients.
    • Ensuring that any confidential information or personal data related to ProPharma, and its clients is managed in accordance with Data Privacy regulations as described in ProPharma Standard Operating Procedures (SOPs)
    • Working in a professional manner at all times with clients, customers, team members and management.
    • Other duties as assigned.

    Qualifications

    • Pharm D graduate
    • Excellent written communication skills
    • Computer literacy.
    • Sound planning, prioritising and organisational skills.
    • Excellent accuracy and attention to detail.
    • Able to work within a team in an open and professional manner.


    Disclaimer: This job posting & Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    BIOTECHpharmacovigilanceclinical researchservice deliverydata privacymedical writingPharm DHealthcareQuality AssuranceResearchCommunication SkillsLiteratureEquityLegalcompliancePharmaceuticalArtificial Intelligence

    About ProPharma Group

    ProPharma Group logo

    ProPharma Group

    Clinical Research

    100

    employees

    2001

    25 years old

    Hyderabad / Secunderabad, Telangana

    India

    ₹8.3L PA avg

    Avg at ProPharma Group

    About

    We are #soaringbeyondCRO as the World’s Largest RCO

    Industries

    Clinical Research

    Employee ratings

    10 reviews

    4.2/ 5

    Culture

    4.7

    Career growth

    4.1

    Work-life

    4.9

    Employees rate it well for

    Work-Life Balance43Skill Development43

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    Medical Information Writer · waiting for your command