Scientific Advisor Rare Disease & General Medicine

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 Affairs

Job Category:
Scientific/Technology

All Job Posting Locations:
Toronto, Ontario, Canada

Job Description:

We are searching for the best talent for Scientific Advisor Rare Disease & General Medicine located in Toronto, Ontario, Canada.

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

Purpose:

Scientific Advisor will be responsible for providing expert scientific expertise in the Rare Disease & General Medicine therapeutic areas while managing a broad range of Medical Affairs activities, as assigned by the Medical Director, including scientific data management, publication plan, training and support of the MSL team, and establishing and maintaining trusted relationships with relevant Key Opinion Leaders (KOLs).

You will be responsible for:


* Establish and maintain trusted peer-to-peer relationships with specific KOLs to collaborate on scientific projects, share balanced scientific data as needed, and provide support in the development of clinical publications in accordance with company policies, applicable laws, regulations and ethical standards.


* Provide strategic scientific support to key stakeholders, including Marketing, Access and Regulatory Affairs.


* Critical contributor to study design, protocol development, and interpretation of results, post-hoc analyses and publication for local company sponsored phase IV programs.


* Lead the process for execution of the local clinical trial initiatives within the therapeutic areas.


* Identify new development trends most likely to impact the business and devise plan of actions to innovate or close the scientific gaps.


* Lead the development and/or review/approval of balanced and credible communication materials (including slide presentations) for internal and external use and dissemination and provide congress support.


* Develop and/or deliver scientific training for internal partners and MSL team.


* Accountable for regular review, analysis and dissemination of medical ...