VP of Clinical Affairs

Job description

The VP of Clinical Affairs will be responsible for the company’s clinical activities, including site management and patient enrolment. The VP of Clinical Affairs will provide instruction

and oversight to the sites in Europe and North-America.

The ideal candidate should be comfortable working in a dynamic, fast-paced,

multidisciplinary environment.

This position will report to the Chief Regulatory and Clinical Officer. This is a full-time, on-site role

Responsibilities:

• Manage Company’s clinical trials

• Support regulatory submissions for study approval

• Assist with contract and budget negotiations with sites

• CRO management

• Routine clinical and project management activities throughout the study:

• Site support and training

• Patient recruitment and site motivation

• Direct contact with clinical sites

• Identify, evaluate, and recruit clinical specialists/field engineers

• Clinical supply management (devices and accessories)

Qualifications:

• BSc/MSc or higher in life science, medicine or a similar field

At least 5 years of experience in Leading clinical affairs within a medical device

company

• Excellent communicator with strong interpersonal skills

• Demonstrated project management skills

• Knowledge of regulatory submission and approval processes

• Fluent in verbal and written English

• Ability to travel frequently – at least once per month

Location: Center District, Israel