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Scientific Writer

Russell Tobin

United Kingdom

Remote

GBP 40,000 - 60,000

Full time

Yesterday
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Job summary

A leading company in the pharmaceutical sector is seeking an Expert Scientific Writer to manage high-quality medical communications deliverables. The ideal candidate will have a strong scientific background, proven medical writing experience, and the ability to communicate complex concepts effectively. This remote role requires flexibility and a commitment to quality standards in deliverables.

Qualifications

  • Minimum of 5 years’ experience in medical communications.
  • Medical writing experience required.
  • Understanding of industry publication processes.

Responsibilities

  • Manage and complete assigned Medical Communications deliverables.
  • Research and write original content for publication activities.
  • Prepare meeting materials and reports.

Skills

Scientific writing
Analytical thinking
Creative problem-solving
Medical accuracy
Time management

Education

Science degree or equivalent
MSc, PhD, PharmD, or MD

Tools

Microsoft Office Suite

Job description

Direct message the job poster from Russell Tobin

Senior Associate @ Russell Tobin || MBA in Human Resources || Recruitment

Job Title: Expert Scientific Writer

Location: UK and Ireland (Remote)

To manage and complete assigned Medical Communications deliverables at high quality standards and in accordance with agreed timelines. Projects include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning and medical education materials for internal medical and/or clinical teams.

  • Demonstrate a command of assigned therapeutic areas and expertise with assigned products.
  • Research and write original content for publication activities (primary and secondary manuscripts, review articles, abstracts, posters), slide presentations, and other materials based on direction and materials supplied by customers.
  • Prepare meeting materials for satellite symposia (agenda, slide content, speaker briefings etc.), and reports from advisory boards and other internal or external meetings.
  • Develop content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards for author review, customer review as appropriate, and scientific peer review.
  • Perform quality control (QC) checking / proofreading as needed.
  • Clearly communicate medical scientific concepts in a condensed, audience-appropriate way.
  • Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3.
  • Be flexible/adaptable to work across therapeutic teams and multiple brands.
  • Interpret and apply clinical data in deliverables.
  • Develop and adhere to timelines with service team and line manager.
  • Aid in troubleshooting/problem-solving.
  • Collate and incorporate author/customer comments.
  • Lead and/or participate in author/client teleconferences.
  • Provide accurate citations and references using the Reference Manager system.
  • Participate in strategic and tactical publications planning and related research.
  • Work collaboratively; mentor junior colleagues when required.
  • Support people and performance management.
  • Maintain records for assigned projects including archiving.
  • Ensure compliance with audit, SOP, WP, and training.
  • Perform additional work-related tasks as assigned. ️ Travel may be required.

Adheres to quality, timeliness, and productivity of deliverables

Strong scientific and medical accuracy in writing

Creative and strategic problem-solving

Solid analytical thinking, planning, and execution

Highly organized and capable of multitasking

Flexible and able to adapt under time constraints

Proven track record of high-quality outputs

Knowledge of GPP3

Alignment with Company values and behaviors

Ideal Background:

Education:

Minimum: Science degree or equivalent

Desirable: MSc, PhD, PharmD, or MD

Minimum of 5 years’ experience in medical communications

Medical writing experience

Understanding of industry publication processes

Proficient in Microsoft Office Suite

If you're an experienced medical writer with a scientific mindset and a passion for impactful communication, we want to hear from you!

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Research, Science, and Writing/Editing
  • Industries
    Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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