At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world.
With our Paradise™ uRDN System, we’re on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure.
Join us on our journey and make a meaningful impact on the lives of people around the globe.
The Director, Medical Device Safety will be responsible for leading global safety and imaging for clinical and commercial use of Recor Medical products.
Responsibilities include managing a growing team of physicians and scientists who support Safety and Imaging teams.
The position requires experience leading and developing vigilance/safety reporting processes globally and developing/managing teams to support those goals.
This position requires device and medical safety background within clinical trials and commercially.
The position will work cross-functionally with the global organization.
Managers in Clinical Safety and Clinical Imaging will report into this position.
The position reports to the Vice President, Medical Affairs.
Responsibilities including but not limited to:
Develop global vigilance/safety reporting processes and a team to support those goals
Responsible for oversight of Clinical Safety Team and Imaging Team
Lead and support clinical safety and imaging team managers
Responsible for the monitoring, signal detection, analysis, interpretation, and documentation of medical safety information including safety events, literature, and other sources
Ensure timely and appropriate global reporting of clinical and commercial products
Manage governance goals (DSMB, Imaging Corelab, independent adjudicators, and others)
Responsible for strategic safety and imaging communication to cross-functional ReCor teams
Participates in strategic decision making for maintaining and developing global safety database
Support writing, review, and submission of ad hoc reports, narratives, IFU, annual/quarterly reports, CER, PMCF, PSUR
Manage Health Hazard Assessments
Support Medical Affairs safety guidance to internal and external teams
Perform medical risk benefit assessments and provide support to Quality Affairs and R&D
Align ReCor Medical Affairs with global/Otsuka Medical Devices
Promote a growth environment
Requirements:
Minimum of a MD, DO, MBBS, PhD
Minimum of 3-5 years medical safety and vigilance with knowledge of US, European, and other global regulations
Experience with post market safety surveillance is a plus
Experience in medical devices or combination products is strongly preferred
Strong collaboration skills with cross functional teams
Strong critical thinking skills
Ability to work independently
Strong communication and presentation skills
Active Medical license preferred
Located within commutable distance to Palo Alto with the ability to be onsite 5 days per week (minimum of 3 days per week).
Commensurate with experience, skills, education and training.
COVID-19 vaccination requirements
At Recor Medical, we care, we collaborate, we challenge, and we create.
Pursuant to these core values, we are focused on the health and safety of our employees, as well as the teamwork essential for innovation of our pioneering technology.
COVID-19 vaccines will be required for all ReCor US office employees effective June 10, 2021, as well as all new US office employees joining our company.
Fully vaccinated persons are those who are >=14 days post-completion of the primary series of an FDA-authorized COVID-19 vaccine.
Equal Employment Opportunity
At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients.
As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
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