Covance

  • MEDICAL WRITER I, LEEDS

    Job Location(s) UK-Leeds
    Job Number
    2018-22186
    Job Category
    Clinical Operations
    Position Type
    Full-Time
  • Job Overview

    COVANCE

     

    As an integral part of everything we do, our employees make a difference in the lives of millions of people… and you will too.

     

    If you want to accelerate your Medical Writer career, think long-term and the extraordinary possibilities we can offer you at Covance. We have helped the pharmaceutical industry develop:

    • More medicines worldwide than any other company, including the top 50 best-selling drugs on the market today, and
    • 100 % of all Oncology drugs approved in 2016.

    Covance’s early clinical business is unique in the industry because it includes an extremely diverse and challenging set of studies (typical phase I healthy volunteer studies through Phase II proof of concept).

     

    Our medical writing team is exposed to a variety of study designs, endpoints, molecules, and clients. We offer the opportunity to develop clinical pharmacology skills that most other medical writing employers do not offer.

     

    The challenges of our study opportunities combined with the diverse role make the position a unique opportunity for someone to develop a broad knowledge base and skill set.

     

    Explore this Medical Writer job with us and check for yourself why Covance is known to promote 2.5x more employees annually than the average company in the biopharmaceutical sector.    

     

    THE JOB

     

    Ideally based at our office in Leeds city centre; however, we will consider home based working.

     

    In this job, you will typically work on clinical documents for studies in the early phases of clinical development (e.g., Phase I through IIa studies).

     

    We will trust you to independently prepare clinical study protocols and clinical study reports (CSRs), and other regulatory documents as needed.

     

    You will interpret clinical, pharmacokinetic, pharmacodynamic and statistical data, and will be responsible for writing the results for these data.

     

    You will ensure timely delivery of high quality documents to internal customers and Sponsors.

     

    You will foster excellent working relationships with all clients (both internal and external), with the highest quality of service in a cost-effective manner on time, every time.

     

    Join us and see why Covance has been named among the World´s Most Innovative Companies in Forbes´ 2017 Ranking, and more than 90% of the top 20 global pharmaceutical companies are repeat customers… we can offer you not only a job, but a stable, long-term international career.

     

    Education / Qualifications

    You are educated in one of the Life Sciences, ideally to an advanced degree such as Master´s, PhD or PostDoctoral Research.

    Experience

    You bring some medical writing experience at a CRO or Bio-Pharmaceutical company.

     

    In lieu of the above, you have strong scientific writing and scientific data interpretation skills.

     

    You will have direct contact with our external clients, so excellent interpersonal and communication skills are needed.

     

    Excellent command of written and spoken English

     

    Good written and verbal communication skills

     

    In-depth knowledge of MS Word

     

    Good organizational and time management ability

     

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