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    Associate Medical Writer Opportunity at Allucent – Pharma Candidates Apply

    Build Your Career as an Associate Medical Writer job at Allucent Careers | Apply Now

    Start your journey into regulatory and scientific writing with Allucent through their Associate Medical Writer role, an ideal starting point for those seeking Medical Writer Jobs, exploring Allucent Careers, or looking to grow in Scientific Writer Jobs within global drug development. This position offers hands-on experience in CMC, nonclinical, clinical, medical, and regulatory writing while providing mentorship and professional growth in a collaborative scientific environment.

    Job Details:

    • Job Title: Associate Medical Writer
    • Location: Not Specified

    About The Company:

    Allucent Regulatory Consulting is a leader in providing comprehensive consulting and solutions to the pharmaceutical and biotechnology industries. Our commitment to excellence and innovation ensures that we deliver the highest quality regulatory support to our clients worldwide.

    Job Description | Medical Writer Jobs

    The Associate Medical Writer assists in writing, editing, and compiling written deliverables in the disciplines of chemistry, manufacturing, and controls (CMC), nonclinical, clinical, medical, and regulatory for submission to regulatory agencies of Allucent Regulatory Consulting. This position develops skills in scientific discussions regarding the planning, production, and review of written deliverables. The Associate Medical Writer is a member of the medical writing staff.

    Key Responsibilities in a Medical Writer Job:

    • Assists with writing, editing, and compiling written deliverables in the disciplines of CMC, nonclinical, clinical, medical, and regulatory for submission to regulatory agencies (e.g., U.S. Food and Drug Administration), sponsor use, or for publication or presentation.
    • Contributes to scientific discussions regarding the planning, production and review of written deliverables.
    • Develops knowledge of applicable regulatory agency requirements and guidance, ICH Guidelines, and other industry best practices.
    • Develops knowledge of company templates, requirements, and resources related to the production of written deliverables.
    • Assists in the development of templates and guidelines for regulatory and other written deliverables.
    • Performs literature searches as applicable.

    Requirements

    • Assists with writing, editing, and compiling written deliverables in the specified disciplines for submission to regulatory agencies, sponsor use, or for publication or presentation.
    • Contributes to scientific discussions regarding deliverable planning, production, and review.
    • Applies company policies and procedures to resolve a variety of issues.
    • Contributes to evaluation/improvement of processes and procedures within the Quality Management System.
    • Assures good communication and relationships with clients.
    • Contributes to other business areas as required.
    • Works in an office environment with minimal travel involved.

    Qualifications Required For Allucent Careers:

    • B.S., or equivalent degree, in a scientific area; M.S., Ph.D., Pharm.D., M.D., or equivalent degree preferred.
    • Up to 1 year of directly relevant work experience post-degree, including medical writing experience.
    • Proficiency with Word, Excel, and PowerPoint required.
    • Good interpersonal, written, and verbal communication skills.
    • General regulatory and scientific knowledge of drug, biologic, or device development.

    Skills

    • Writes, edits, and compiles deliverables with autonomy commensurate to experience.
    • Adheres to regulatory practices and company guidelines as directed.
    • Awareness of contract and budget specifications with effective communication of changes.
    • Interacts with various departments to facilitate completion of deliverables.
    • Seeks opportunities for professional development.

    Benefits

    • Comprehensive benefits package per location.
    • Competitive salaries per location.
    • Departmental Study/Training Budget for professional development.
    • Flexible Working hours.
    • Leadership and mentoring opportunities.
    • Participation in our Buddy Program.
    • Internal growth opportunities and career progression.
    • Financially rewarding internal employee referral program.
    • Access to online training via GoodHabitz and internal platforms.
    • Eligibility for Spot Bonus and Loyalty Award Programs.

    CLICK HERE TO APPLY

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