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    Medical Writer 1

    Fortrea
    0-2 years
    Not Disclosed
    Remote, USA
    10 Nov. 15, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Position: Medical Writer 1
    Company: Fortrea

    About Fortrea:

    Fortrea, a global leader in contract research, is dedicated to advancing clinical development in partnership with pharmaceutical, biotechnology, and medical device industries. Operating in over 90 countries, Fortrea is committed to transforming drug and device development, enabling life-changing therapies to reach patients worldwide.

    Role Overview:

    Are you passionate about scientific writing and clinical research? Join Fortrea as a Medical Writer 1 and play a crucial role in creating clinical documents for early-phase trials (Phase I-IIa), with a focus on safety and pharmacokinetics. In this role, you’ll collaborate across teams to ensure new treatments are safe for patients, while also launching a global career in clinical trials.

    Location:

    • Hybrid Model: Blend remote work with in-office presence for collaboration and training.
    • Leeds, UK: Work in a state-of-the-art Phase I clinical facility, conveniently located just minutes from the train station.

    Key Responsibilities:

    • Learn and Grow: Gain hands-on experience in medical writing and clinical trial documentation.
    • Document Development: Develop Protocols and Clinical Study Reports (CSRs) under supervision, mastering the document development lifecycle.
    • Data Analysis and Reporting: Review and interpret pharmacokinetics and safety data, condensing findings into clear, concise reports.
    • Project Management: Coordinate with cross-functional teams and ensure alignment with sponsor goals, study timelines, and milestones.
    • Client Engagement: Set expectations, manage feedback, and lead discussions with clients in the pharma and biotech sectors.

    Ideal Candidate Profile:

    • Educational Background: Bachelor’s degree in biomedical, life sciences, or a related field.
    • Experience: Previous experience in medical writing within CRO, Pharma, or Biotech is preferred. However, strong scientific writing, data analysis, and attention to detail—gained through a PhD or fast-paced research setting—are also valuable.
    • Key Skills: Proactive communication, comfort with regulatory documents, and the ability to handle shifting priorities and deadlines.

    Why Fortrea?

    At Fortrea, you’ll find:

    • Diverse Career Paths: Training and growth opportunities tailored to your aspirations.
    • Supportive Environment: Comprehensive training, management support, and access to experts in the field.
    • Growth Potential: Your career journey, whether as a medical writer or in leadership, is nurtured by our team’s commitment to your professional development.

    Join us and be part of a team dedicated to revolutionizing clinical trials. Apply now to make a global impact with Fortrea.

    Equal Opportunity Employer:

    Fortrea is an Equal Opportunity Employer, committed to diversity and inclusion. Employment decisions are based on qualifications and business needs without discrimination based on race, gender, age, disability, or other protected status. We encourage all qualified applicants to apply.

    For more information, visit www.fortrea.com.

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