Senior Analyst, Oncology 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:
Spring House, Pennsylvania, United States of America

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 https://www.jnj.com/innovative-medicine

Please note that 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 of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Europe - Requisition Number: R-001291

Canada - Requisition Number: R-002012

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

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

We are searching for the best talent for Senior Analyst, Oncology Medical Writing to be in North America, Europe, or other global locations.

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:


* Writes or coordinates clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.


* Leads cross-functional (eg, with clinical team) document planning and review meetings.

Interacts with cross-functional colleagues on document content and champions MW processes and best practices.

Responsible for establishing document timelines and strategies in accordance with intern...