Manager, Oncology Regulatory Medical Writing

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. Learn more at https://www.jnj.com

Job Function:
Medical Affairs Group

Job Sub Function:
Medical Writing

Job Category:
Professional

All Job Posting Locations:
US063 NJ Raritan - 920 US Hwy 202

Job Description:

Manager, Oncology Regulatory Medical Writing

At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives.

We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.

Johnson & Johnson Innovative Medicine discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiopulmonary, and retina.

Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team are recruiting for a Manager to support our Oncology therapeutic area.

The position is located in the United States.

Remote work options may be considered on a case-by-case basis and if approved by the company.

Are you ready to join our team? Then please read further!

Key Responsibilities:



* Prepare and finalize all types of clinical documents.


* Lead in a team environment.

Work with a high level of independence and take a lead role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking.


* Lead or set objectives for others on team projects and tasks, eg, lead process working groups.


* Guide or train cross-functional team members on processes and best practices.


* May lead project-level/submission/indication writing teams.


* Proactively provide recommendations for departmental process improvements.


* If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team.

Responsible for planning and leading the writing group for assigned program.


* Actively participate in medical writing and cross-functional meetings.


* Maintain knowledge of industry, company, and regulatory guidelines.


* Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the work of other medical writers, external contractors, and document specialists supporting a project.


* May interact with senior cross-functional colleagues to strengthen coordination between departments.


* May represent Medical Writing department in industry standards working groups.


* If a p...