Associate Director, Clinical Science & External Research

Johnson & Johnson is currently seeking an Associate Director, Clinical Science & External Research (CSER) to join our Biosense Webster team located in Irvine, CA

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/ .

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.

Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The Clinical Science & External Research (CSER) Associate Director will drive end-to-end evidence generation and dissemination strategies (EGS/EDS).

In collaboration with cross-functional teams and research investigators, the CSER manager will generate clinical evidence for the company's pipeline that impact patient lives.

This role will have broad reach and visibility with international team members!
Key Responsibilities :


* Leads evidence generation and dissemination strategy for strategic portfolio, including developing and implementing publication plan


* Leads publication development in partnership with Clinical Research, Biostatistics and physician authors


* Provides critical scientific input to publications


* Manages non-regulated studies (investigator initiated, registries, real-world evidence or company sponsored post-market studies) and regulated studies (post-approval, real-world evidence)


* Develops study protocol for assigned studies


* Provides input to company-sponsored studies protocol development as needed


* Develops positive relationship with diverse cross-functional teams including Medical Affairs, Health Economics and Market Access, Global Strategic Marketing, Biostatistics etc.


* Leads external scientific discussions and builds positive relationships with external physician partners


* Leads or participates in monthly literature review with global teams; performs literature review as needed to support EGS and EDS


* Handles budget assoc...