ABBOTT LABORATORIES Regulatory Medical Writer Salary in the United States

How much does a Regulatory Medical Writer make at companies like ABBOTT LABORATORIES in the United States? The average salary for Regulatory Medical Writer at companies like ABBOTT LABORATORIES in the United States is $89,193 as of May 28, 2024, but the range typically falls between $76,808 and $101,578. Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, helps you determine your exact pay target.  View the Cost of Living in Major Cities


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What does a Regulatory Medical Writer do at companies like ABBOTT LABORATORIES?

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries.

Develop and write Clinical Evaluations Plans and Reports for new and existing medical devices; Provides scientific/clinical expertise throughout the development and implementation of clinical evaluations and other risk management deliverables. Work with cross-functional teams and independent medical experts to develop clinical evaluation deliverables

Core Job Responsibilities

  • Responsible for writing Clinical Evaluation Plans/Reports and other clinical deliverables by evaluating clinical evidence such as, clinical investigation, literature and post-market surveillance data
  • Ensures quality by following procedures, work instructions and templates
  • Drafts forms/templates for successful preparation of robust CERs and other documents
  • Assists with other clinical, regulatory, quality and engineering projects as assigned
  • Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management as directed
  • Creates or manages timelines of deliverables
  • Interprets results in preparation for product applications by evaluating clinical and scientific and risk data and literature

Preferred Skills and Experience: 

  • At least 3 years of regulatory, medical or scientific writing experience; CER writing experience preferred
  • Excellent written and verbal communication skills. Experience in working with collaborative, cross-functional teams.
  • Scientific/research background (i.e., has understanding of research design, methodology, and statistics)
  • Excellent analytical skills
  • Ability to manage complex tasks and manage time efficiently
  • Proficient computer skills with Word, Excel, PowerPoint, Outlook, etc.
  • Attention to details.

Minimum Education

  • Bachelor's degree required, advanced degree preferred. Degree in the sciences, medicine, or similar discipline highly preferred.
$76,808 Low Average $89,193 High $101,578

Understand the total compensation opportunity for Regulatory Medical Writer at companies like ABBOTT LABORATORIES, base salary plus other pay elements

Average Total Cash Compensation

Includes base and annual incentives

The chart shows total cash compensation for the ABBOTT LABORATORIES Regulatory Medical Writer in the United States, which includes base, and annual incentives can vary anywhere from $76,808 to $101,578 with an average total cash compensation of $89,193. Total compensation includes the value of any benefits received in addition to your salary and some of the benefits that are most commonly provided within a total compensation package including bonuses, commissions, paid time off, and Insurance. The total cash compensation may get paid differently by industry, location, and other factors.
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