Medical Writer III

Other

Posted 13 days ago


Job description

Job Description:
The Fact Checker (Medical Writer III) works closely with Medical Writers to confirm that supplied references adequately support claims being made in pharmaceutical advertising materials focused on oncology, neuroscience, immunology, and specialty products. The Fact Checker verifies clinical and other data and creates annotated reference documents that outline where claims are located in published sources to facilitate Veeva PromoMats project submission and Medical/Regulatory/Legal review.
Responsibilities:
  • Checks claims in advertising and promotional documents against published sources before projects are submitted for Medical/Regulatory/Legal review.
  • Ensures that suitable references are used to support all product and promotional claims in text, graphs, charts, tables, and statistical analyses.
  • Creates annotated documents to be used for submitting/linking projects in Veeva Promo Mats
  • Works with writers, editors, account managers, and Veeva submission specialists to ensure project submissions are accurate, current, and compliant.
  • May be asked to research promotional claims and perform data mining, working with Clinical Study Reports (CSRs) and resources from the client Library.
  • Organizes and manages approved references.
  • Links claims to be published sources in Veeva Promo Mats, as needed.
Requirements:
  • Bachelor's degree or higher in a medical-related field (eg, biology or chemistry])
    or equivalent experience within the pharmaceutical or related industry.
  • 3+ years of medical fact checking experience; advertising agency experience a plus.
  • Expertise in oncology and/or neuroscience fields a plus.
  • Proven ability to research, understand, and interpret medical and scientific data.
  • Working knowledge of regulations and standards related to promotion of pharmaceutical products and AMA style guidelines.
  • Proficiency in Adobe Acrobat Pro and MS Word; familiarity with Veeva Vault a plus.
  • Ability to work in fast-paced environment and juggle multiple deadlines without sacrificing quality or accuracy.
  • Analytical thinker and proactive problem solver.
  • Ability to work independently and collaborate with team members, as needed.
  • Advanced written, verbal, time management, and organizational skills.
Top Skills:
  • Experience fact checking medical claims against published sources.
  • Proven ability to research, understand, and interpret medical/scientific data.
  • Strong attention to detail; organized.
  • Ability to work quickly without sacrificing accuracy/quality.
  • Exceptional communication skills, ability to work well across multiple teams.
  • Ability to manage multiple deadlines, work well under pressure.
  • Proficiency in Adobe Acrobat annotation tools.
  • BA/BS preferably in medical-related field (eg, biology or chemistry) or equivalent business experience within the pharmaceutical or related industry.
Nice to have:
  • Experience in pharma advertising industry.
  • Experience with Veeva Promo Mats and/or OPDP submissions a definite plus.
  • Science background and/or knowledge of medical terminology a definite plus.
  • Experience with medical copyediting a plus.

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About Katalyst Healthcares & Life Sciences

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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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Frequently asked questions

Q: What skills or qualities help someone succeed as a Medical Writer?

A: To succeed as a Medical Writer, key technical skills include a strong understanding of medical terminology, pharmacology, and regulatory guidelines such as FDA regulations and ICH guidelines. Soft skills like excellent communication, attention to detail, and the ability to distill complex scientific information into clear, concise language are also crucial. These strengths enable Medical Writers to effectively convey critical information to various audiences, from healthcare professionals to patients, and support their career growth by fostering a reputation for accuracy and clarity.

Q: What is the career path for a Medical Writer?

A: A Medical Writer's typical career progression involves starting as an Entry-Level Medical Writer, where they assist in creating content for pharmaceutical companies, medical device manufacturers, or healthcare organizations. As they gain experience, they can move into Mid-Level roles such as Senior Medical Writer or Medical Communications Specialist, where they lead content development, manage teams, and develop strategic communication plans. Ultimately, Senior Medical Writers can advance to roles like Medical Director or Scientific Communications Lead, overseeing large-scale content initiatives and mentoring junior writers, or transition into related fields like Regulatory Affairs, Clinical Research, or Science Publishing.



Katalyst Healthcares & Life Sciences job posting for a Medical Writer III in Mettawa, IL with a salary of $35 to $58 Hourly with a map of Mettawa location.