Associate Medical Director

The Company

The world's largest medical device company dedicated to less-invasive therapies. They are committed to improving the quality of life for patients, their families and their loved ones. This company has maintained the same mission of improving the quality of patient care and the productivity of health care delivery for over two decades. It is of the utmost importance throughout the Company that all employees understand the difference they make in countless lives. A global company with people of many cultures in many countries, who speak many languages and who share one belief: together they can change health care for the better, not just for a few patients, but for thousands around the world. In the end, it all comes down to people.

Scope of the Job

The Associate Medical Director located in Massachusetts, reports to the Medical Director, Clinical Scinences. Your basic role will be to:

Provide medical and scientific expertise in the area of cardiovascular imaging including IVUS, intra-coronary Doppler & flow. The mandate of the associate medical director is as follows:

To maintain timelines by providing high level medical/therapeutic guidance to internal and external customers including project teams, functional units, investigators, and regulatory agencies.

To provide early, hands-on operational support to teams in clinical trial planning, protocol development, investigator selection, training of internal and external personnel, medical monitoring for trial safety, and quality control.

You will be responsible for providing cardiovascular imaging area expertise to support development and execution of clinical trials in device development process.

In addition you will be responsible for review and editing of protocols to insure accuracy, consistency with standard of care, logistical ease, and internal consistency. To provide direct physician support to quality assurance group for review of product complaints, MDR reporting criteria, health risk assessments, and product performance criteria.

Writing/editing of clinical reports for regulatory submission and updates to insure medical accuracy. Provide medical monitoring to insure patient safety and adequate reporting and coding of adverse events in clinical trials.

Candidate Requirements:

We seek candidates with 5 Years clinical experience in interventional cardiology, excellent oral and written communications skills.

Candidates should have experience in writing scientific reports with strong organizational and interpersonal skills.

Candidates should be willing to travel up to 40%

We seek candidates with evidence of a management style characterized by leadership, vision, collegiality, teamwork, preparation and communication. In addition, a self-confident, analytic, intelligent, strategic thinker with the highest personal integrity is sought after.

Compensation

A compensation package will be designed to attract outstanding talent and includes a base salary, bonus, 401K, stock options and other standard benefits.

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