At a Glance
- Tasks: Write and coordinate clinical documents that save lives in oncology.
- Company: Join Johnson & Johnson, a leader in healthcare innovation.
- Benefits: Competitive salary, hybrid work model, and inclusive culture.
- Other info: Collaborative environment with opportunities for mentorship and career growth.
- Why this job: Make a real impact on patient health through innovative medical writing.
- Qualifications: 6+ years in pharma with regulatory writing experience; oncology knowledge preferred.
The predicted salary is between 87000 - 140300 $ per year.
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 MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
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.
We are searching for the best talent for Medical Writer III, Regulatory Medical Writing to support Oncology within our Integrated Data Analytics & Reporting (IDAR) business. The position may be located in Toronto, Canada or other locations. The position is Hybrid (3 days onsite weekly). Remote work options may be considered on a case-by-case basis and if approved by the company.
Purpose: Able to write and coordinate basic and complex documents, independently when working within own therapeutic area (TA), and under supervision when working across TAs. Leads in a team environment and matrix. Able to function as a lead MW on most compounds, under supervision. Actively participates in or leads process working groups. Provides input into functional tactics/strategy (eg, writing teams, process working groups). Highly proficient in the use of internal systems, tools, and processes.
You will be responsible for:
- Writing or coordinating clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.
- Leading cross-functional document planning and review meetings.
- Interacting with cross-functional colleagues on document content and championing MW processes and best practices.
- Establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.
- Completing all time reporting, training, metrics database, and project tracking updates as required in relevant company systems.
- Coaching or mentoring more junior staff on document planning, processes, and content.
- Providing peer review as needed.
- Actively participating in or leading process working groups.
Principal Relationships:
- Internal: manager, other writers, cross-functional contacts involved in the preparation and planning of clinical documents.
- External: May interact with or oversee day-to-day work by contractors or external service providers as needed under supervision.
Education and Experience Requirements:
- A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) is preferred.
- At least 6 years of relevant pharmaceutical/scientific industry experience including at least 4 years of regulatory medical writing experience.
- Oncology therapeutic area experience is preferred.
- Proficiency in written and spoken English is essential.
- Able to build solid and positive relationships with cross‐functional team members.
- Strong leadership skills, both in project and process management as well as in time management.
- Demonstrate learning agility and mentoring competency.
- Strong attention to detail.
Benefits: The expected base pay range for this position is $87,000 to $140,300 CAD.
Medical Writer III, Oncology in Toronto employer: Biopharma Careers
At Lilly Canada, we pride ourselves on fostering a collaborative and innovative work culture that empowers our Medical Science Liaison team to make a meaningful impact in the fields of Immunology, Gastroenterology, and Rheumatology. Our commitment to employee growth is evident through continuous learning opportunities, competitive compensation packages, and comprehensive benefits, including participation in the Lilly Bonus Program and flexible healthcare options. Located in Western Canada, our team enjoys a supportive environment that values scientific exchange and encourages building strong relationships with the medical community.
