Manager, Clinical Science & External Research

Biosense Webster Inc.

is recruiting a Manager, Clinical Science & External Research (Scientific Communications) located in Irvine, California.

This role will work a hybrid schedule and must live within a commutable distance to Irvine, CA to report to the office on assigned days 2-3 times per week.

The Manager, Clinical Science & External Research (CSER) will be responsible for leading and developing internal and external scientific communication contents for assigned projects.

We are looking for someone with high standards of scientific analysis, teamwork, creative thinking, and interpersonal skills for the advancement of clinical programs via evidence generation and dissemination.

You will collaborate closely with a cross-functional team, including Scientific Affairs, R&D, Health Economics, Marketing, and Education to conduct literature reviews and gap analyses, lead strategic analysis of scientific data, craft and implement comprehensive publication plans, and support internal and external scientific communication plans for various target audiences.

In collaboration with cross-functional teams and research investigators, you will generate clinically relevant evidence for the company's innovative pipeline that impacts patient lives.

You will be joining a growing function that drives research innovations! This role will have broad reach and visibility with the Company.

You should possess advanced understanding and maintain current knowledge of industry standards on scientific communication and publication development.

You will demonstrate understanding of the disease area, develop a keen understanding of the Operating Company product portfolio and clinical strategies to provide strategic input to publication planning & evidence generation and dissemination strategies.

We are looking for a highly motivated and independent individual with abilities to problem solve and run projects effectively.

You are expected to provide quality feedback and keep management informed of key developments and issues related to your projects.

You will understand, incorporate, and follow all applicable laws and regulations related to business activities, and Policies and Procedures of Healthcare Compliance and Code of conduct.

You will serve as an internal subject matter expert on guidelines governing the ethical publication of clinical study data, including mastering the guidelines set forth by the International Committee of Medical Journal Editors and Good Publication Practices, and applicable policies governing compliant scientific communications.

You may be asked to provide training for employees, as needed.

Additionally, you may support associates that handle a variety of clinical studies (investigator Initiated, registries, real-world evidence or company sponsored post-market studies/premarket collaborative studies) that collectively drive the generation of clinical evidence for the Company's portfolio.

You will consistently strive to improve the performa...