Senior Director, 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:
People Leader

All Job Posting Locations:
Titusville, New Jersey, 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

The primary work location for this role is Titusville, NJ.

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

Position Summary:

The Senior Director, Regulatory Medical Writing (Reg MW) is a highly experienced and influential leader with expert knowledge of Reg MW strategic concepts and processes.

This role is accountable for the strategic and operational leadership of Reg MW activities.

This role requires a well-established leader, with a recognized track record of substantial organizational development and leadership, assuring efficient production and quality of all Reg MW deliverables.

This role has independent decision-making authority for decisions that could have significant/long-term impact on the direction and effectiveness of the Reg MW organization.

This position reports to the Head of Reg MW and is expected to be capable of representing Reg MW in a leadership capacity.

The role requires strong partnership and close collaboration with senior functional and matrix leaders across the Innovative Medicine R&D (IMRD) organization to ensure the successful, efficient, high-quality and compliant portfolio delivery.

Principal Responsibilities:

Leadership:


* Member of the Reg MW Leadership Team, reporting into the Global Head of department.

Help establish the strategy and direction of Reg MW and maximize medical writing effectiveness and productivity.


* Responsibility for functional leadership with high material impact in strong competitive landscape.

Able to navigate complex organizational structure and act as Reg MW interface for respective Therapeutic area and Delivery Unit.


* Strategic leadership accountabilities include driving the development of capabilities and shaping organizational structures across a large and compl...