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Medical Writer II, Oncology

Job in Toronto, Ontario, C6A, Canada
Listing for: Johnson & Johnson Innovative Medicine
Full Time position
Listed on 2026-06-12
Job specializations:
  • IT/Tech
    Medical Imaging
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CAD Yearly CAD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Overview

R-081529

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are positioned to innovate across the full spectrum of healthcare solutions today to deliver breakthroughs of tomorrow, and profoundly impact health for humanity.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered an individual. We respect the diversity and dignity of our employees and recognize their merit.

Job Details

Job Function Medical Affairs Group

Job Sub Function Medical Writing

Job Category Professional

All Job Posting Locations Allschwil, Basel-Country, Switzerland;
High Wycombe, Buckinghamshire, United Kingdom;
Leiden, Netherlands;
Spring House, Pennsylvania, United States of America;
Titusville, New Jersey, United States of America;
Toronto, Ontario, Canada

Job Description

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at

About Oncology

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at

Role

We are searching for the best talent for Medical Writer II, Oncology. This role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all postings, focus on the specific country(s) that align with your preferred location(s):

  • United States — Requisition Number: R-080142
  • Canada — Requisition Number: R-081535
  • Belgium & Netherlands — Requisition Number: R-081529
  • Switzerland — Requisition Number: R-081537
  • United Kingdom — Requisition Number: R-081540

Remote work options may be considered on a case-by-case basis and if approved by the Company. Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Purpose
  • Develops within the medical writing role within the pharmaceutical industry.
  • Works in a team environment and matrix.
  • Performs routine tasks per established procedures.
  • Gains knowledge and applies internal standards, regulatory, and publishing guidelines.
  • With increasing skill, uses internal systems, tools, and processes.
  • Writes and coordinates basic documents, preparing more complex documents (within the TA and across TAs) in accordance with experience level.
  • Functions as a lead writer on a project, indication, or a compound either early- or late-stage in life cycle under close supervision.
  • Participates in process working groups.
You Will Be Responsible For
  • Writes and coordinates basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, table of studies, narratives, and initial IBs.
  • Writes, contributes to, and/or coordinates low to medium complexity clinical and regulatory documents such as Phase 2/3 CSRs and protocols, IB updates, summary documents, and regulatory responses under supervision.
  • Performs document QC, completes list of abbreviations or references, conducts literature searches, and performs other basic tasks with supervision as needed.
  • Participates in and may lead cross-functional document planning and review meetings. Works in a team environment with some guidance while increasing independence for longer-term activities.
  • Takes an active role on assigned projects with respect to timing,…
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