Description

Aidoc is recruiting a Senior Clinical Research Manager in the United States. Join our team!

About Aidoc

Aidoc is a pioneering force in clinical AI. Our clinical AI imaging solutions help physicians quickly identify and diagnose urgent cases and improve patient outcomes. Built on Aidoc’s exclusive aiOS, we analyze and aggregate medical data to enable care teams to operationalize the unexpected and work seamlessly with a continued focus on the patient. Aidoc AI is always on, running in the background to change the foreground.

Our solutions are used in more than 1000 hospitals, including leading health systems in the US. Funded by some of the industry’s leading VC’s, Aidoc has raised more than $250 million to date, and was chosen as one of TIME’s 50 most genius companies.

About this role

This position focuses on developing strategic projects and clinical studies to enhance the clinical credibility of AI in radiology. You will work to develop clinical evidence that promotes our products with scientific rigor. You will work with cross disciplinary teams such as product, data, sales and marketing. You will help define the strategy, study design and processes to proof the value of our solutions. You help create and manage research relationships with customers and key opinion leaders.

Responsibilities

Coordinate activities involved in initiating, monitoring, and completing clinical research studies.
Assist in the identification and recruitment of potential investigators and study sites.
Identify, analyze, and interpret trends or patterns in complex data sets.
Facilitate writing, editing, and preparation of high quality written scientific documents for publications, scientific manuscripts for peer review, white papers, protocols, and other scientific or internal reports.
Assist with submission of protocols for ethics/IRB approval and assist in preparing regulatory submissions.
Conduct scientific literature searches and summarize/synthesize the existing literature in support of publication development.
Assist with drafting protocol-specific manuals, plans, and documents as needed.

Requirements

Bachelors or Masters level degree in a scientific discipline (Clinical Sciences, Health/Life Sciences, Health Economics, or related field)
Proven critical thinking and analytical skills
Ability to search, understand, and synthesize/summarize the existing scientific literature in support of publication development
Ability to interpret tabular and graphical presentations of complex clinical and scientific data and to identify key data points that support strategic goals
Excellent understanding of clinical research design and concepts
Excellent writing skills, with recent history of relevant presentations at scientific conferences and publications in peer-reviewed journals
Medical or scientific writing experience
Basic Data Analysis skills

Working at Aidoc

We’re a dynamic, collaborative and fast growing team of more than 400 global employees, committed to improving the world of healthcare. We’re looking for mission-driven people excited to do transformative work.

We have offices in Tel Aviv, Barcelona and New York City, but Aidoc is a remote-first workplace. We’re able to hire US-based employees across the continental United States, although certain roles may be region-specific.

What we offer:

A range of medical, dental and vision benefits
Stock options for all full-time employees
20 days of paid vacation, plus sick days and holidays
A 401(k) plan, life insurance, plus long and short term disability
The opportunity to directly improve medical care and impact patient outcomes

Aidoc is deeply committed to creating an inclusive and diverse workplace, and to the principle of equal opportunity for all individuals. We prohibit harassment of any type as well as discrimination based on race, color, religion, sex, sexual orientation, national origin, age, disability, veteran status, or any other status protected by law.