Technical Writer - Scientific - II
Listed on 2026-08-03
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Healthcare
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Research/Development
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas:
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Technical and Scientific Reviewer
Summary:
The Technical and Scientific Reviewer provides leadership, motivation, and strategic direction for the scientific and technical content for prepared regulatory documents by the Medical Operations Team. The role is responsible for the review, development, and quality of scientific and medical content and demonstrates an understanding of all assigned therapeutic areas.
Knowledge/Requirements:
- Excellent English language skills, especially writing and proofreading.
- Clinical, scientific or research background, highly preferred.
- Experience writing CERs, highly preferred.
- Knowledge in narrative or systematic literature reviews (e.g. PRISMA, Cochrane), highly preferred.
- Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred.
- Expert understanding of scientific or clinical research and methods.
- Understanding of statistical data and good data management practices.
- Strong oral communication, presentation, project management and prioritization skills.
- Excellent interpersonal relationships.
- Highly proficient in Microsoft Office Suite and bibliographic software (e.g. Endnote, Reference Manager).
Education:
- Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g. medical writing, regulatory affairs, clinical research, engineering)
- BS/B.Pharm/BSN or MS or MPH plus 5 to 10 years of relevant medical device industry experience
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