Associate Medical Writer

hace 2 semanas

Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

The Medical Writing Department of the Global Clinical Trial Operations organization prepares a variety of regulated documentation in support of the clinical development portfolio.

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation.

Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.


The Associate Narrative Medical Writer (MW) is responsible for the development of medical writing deliverables for a limited set of documents within a single therapeutic area under the supervision of management and Principal Medical Writer Safety Lead. The MW supports the clinical development pipeline through scientific contribution of clinical documents related to safety. The MW delivers quality English language documents in compliance with internal conventions and industry standards in a timely and efficient manner following the department and company processes and tools.

The Associate Medical Writer works with guidance and oversight to develop

  • Prepares selected components of regulatory clinical documentation
  • Develops knowledge of regulatory medical writing and therapeutic area/investigational product to support pipeline projects
  • Participates, with supervision, on documentspecific teams
  • Develops competence in writing, editing, and reviewing clinical study reports, patient narratives, investigator brochures, and other clinical regulatory documents per company and other guidelines
  • Acquires a thorough understanding of medical writing responsibilities, including the design, planning, and preparation of clinical documentation in support of clinical development, trials, and sections of filings
  • Identifies challenges associated with medical writing scope of work, seeks advice from management and others as needed, and exercises negotiation and communication skills with project team members
  • May participate in initiatives to improve medical writing processes and standards
Qualifications, Skills & Experience

  • Degree in a life science, preferably related to pharmacy or medicine
  • Bachelor's degree with 2+ years; MS with 1+ year; or doctorallevel degree (e.g., PhD, MD, DVM, DO, PharmD) with 1 year of relevant career experience
  • Demonstrated ability to write scientific documents (e.g., lab reports, publications, dissertations, theses, abstracts)
  • Experience working on teams
  • Technical expertise in typical office Applications (e.g., Microsoft Office, Adobe Acrobat)
  • Demonstrated presentation, writing, and project management skill
  • Proficiency in English
We are a research-driven biopharmaceutical company.

Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world.

We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.


Search Firm Representatives Please Read Carefully

Employee Status:

Project Temps (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

06/4/2024

Job Posting End Date:
06/04/2024

Requisition ID:
R295945

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