Director of Clinical Trials

Job description

The Director of Clinical Trials will be responsible for the company’s clinical activities, including site management and patient enrolment.

The Director of Clinical Trials 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)

Job requirements:

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

• At least 5 years experience in clinical operations 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

• Basic technical skills

• Ability to travel frequently – at least once per month