Analyst II, Regulatory Medical Writing Immunology

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:
Beerse, Antwerp, Belgium, Leiden, Netherlands

Job Description:

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

We are searching for the best talent for Analyst II, Regulatory Medical Writing, Immunology within our Integrated Data Analytics & Reporting (IDAR) business.

The position may be located High Wycombe, UK; Leiden, Netherlands or Beerse, Belgium.

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.

As Analyst II, Regulatory Medical Writing, you will support across the Immunology therapeutic area within our Regulatory Medical Writing team, to author diverse regulatory medical writing documents.

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

Purpose:



* Develop within the medical writing role within the pharmaceutical industry.


* Work in a team environment and matrix.


* Gain knowledge and apply internal standards, regulatory, and publishing guidelines.


* Learn and use internal systems, tools, and processes.


* Write and coordinate basic documents and help to prepare more complex documents.


* Perform routine tasks per established procedures.

You will be responsible for:



* Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator’s brochures with oversight.


* Perform document QC, literature searches, and other tasks.


* Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.


* Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.


* Participate in or lead cross-functional document planning and review meetings independently or with oversight.


* May participate in initiatives to improve medical writing processes and standards.


* Acquire, maintain, and apply knowledg...