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Associate Medical Writer

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor’s/Master’s degree in biomedical or life sciences, Minimum 2 years of industry experience, Knowledge of global regulations (FDA, ICH), Understanding of electronic Common Technical Document (eCTD) requirements.

Key responsabilities:

  • Write, edit, review clinical documentation
  • Track and collect documents for CSR appendices
  • Perform quality control reviews of documents
  • Collaborate with teams on patient safety narratives
  • Act as a backup contact for project managers
PSI CRO AG  logo
PSI CRO AG Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

PSI is a leading Contract Research Organization with more than 28 years in the industry offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description
    • Writes, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation
    • Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives
    • Collects and tracks documents for CSR appendices, in support of the Quality Control Associates and if assigned by the Associate Director, Medical Writing
    • Critically assesses, interprets, and summarizes data from clinical studies
    • Reviews scientific literature pertinent to medical writing activities
    • Performs quality control (QC) reviews of PSI-developed Essential Documents and other documentation (in support of the Quality Control Associates and if assigned by the Associate Director, Medical Writing)
    • Acts as a backup contact for the Project Managers and other PSI functional areas within the scope of assigned medical writing tasks
    • Collaborates with the Process Improvement narrative automation team to develop patient safety narratives

    Qualifications
    • College or university degree, preferably a Bachelor’s/Master’s degree in biomedical or life sciences fields, or a relevant combination of education, training, and experience that presents the required knowledge, skills, and abilities.
    • Minimum 2 years of corresponding industry experience working with clinical documentation and data
    • Prior pharmaceutical, biotechnology, or contract research organization experience
    • Basic knowledge of global regulations and guidelines (FDA, ICH) on the drug development process and on production and publishing of Essential Documents
    • Basic knowledge of electronic Common Technical Document (eCTD) requirements

    Additional Information

    If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

    Required profile

    Experience

    Level of experience: Mid-level (2-5 years)
    Industry :
    Pharmaceuticals
    Spoken language(s):
    English
    Check out the description to know which languages are mandatory.

    Other Skills

    • Quality Control
    • Collaboration
    • Analytical Thinking
    • Verbal Communication Skills

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