Analyst II, Regulatory Medical Writing X-TA

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:
High Wycombe, Buckinghamshire, United Kingdom

Job Description:

Analyst II, Regulatory Medical Writing X-TA

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, X-TA to support across key therapeutic areas (X-TA) 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 including from other EU countries may be considered on a case-by-case basis and if approved by the company.

As Analyst II, Regulatory Medical Writing X-TA, you will support across one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, Specialty Ophthalmology) within our Regulatory Medical Writing team, to author diverse regulatory medical writing documents.

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):

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, an...