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    Job · 11620577

    DAVA Oncology logo

    Medical Writing / Research Analyst

    DAVA Oncology · Not specified · onsite · Posted 69d ago

    Not disclosed1–3 yrsfulltimeSourced fromFoundit

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

    About this role

    Work Hours:U.S. time zones – requires evening/night shifts in India

    DAVA Oncology is a fast-growing oncology-focused consulting company headquartered in Dallas, Texas. We are recruiting for a Medical Writer and Research Analyst to join our team remotely from India. This is a fully remote position, but working hours will be based on U.S. time zones, meaning evening and night shifts will be required.

    Our team members have the opportunity to work in a variety of areas, including but not limited to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable.

    Responsibilities:

    • Conduct secondary research and acquire information from internet sources, compiling it into content.
    • Interpret, analyze, and compile proprietary data in a way that delivers a compelling scientific story.
    • Research, write, edit, and proof protocols, reports, and publications.
    • Maintain a strong scientific understanding of oncology (or the ability to quickly gain such understanding).
    • Prepare materials for major cancer conferences and internal oncology meetings.

    Qualifications:

    • At least 1 year of experience in oncology-focused research or writing is preferred; publication planning experience is a plus.
    • Ph.D. in biology, biochemistry, organic chemistry, immunology, molecular biology, biotechnology, Pharm.D., or other related fields.
    • M.S. degree holders in the above fields with exceptional experience will also be considered.
    • Authorship in prestigious, peer-reviewed journals is highly preferred.
    • Experience in planning, writing, and reviewing study designs, protocols, data analysis, study reports, and regulatory documents is a plus.
    • Industry experience (pharmaceutical companies, CROs, etc.) is highly preferred.

    Skills & Proficiencies:

    • Must be available to work during U.S. business hours (evening/night shifts in India).
    • Strong written and oral communication skills; ability to explain technical concepts clearly.
    • Advanced knowledge of Microsoft Office Suite.
    • Ability to work independently and collaboratively on multiple projects with tight deadlines.
    • Highly motivated, organized, and detail-oriented self-starter.
    • Availability to work U.S. hours (evening/night shifts in India).

    Sourced from foundit

    Skills

    Secondary ResearchMicrosoft Office SuiteStudy Designregulatory documentsdata analysispublication planning

    Medical Writing / Research Analyst · waiting for your command