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Clinical Specialist - Health
AppleCupertino, California, United States$212,000 - $318,4001+ years
Apply Apple Health’s ever-evolving suite of health and wellness products are helping our users live more active, healthier lives. Be ready to make something great when you come here. Dynamic, inspiring people and innovative, industry-defining technologies are the norm at Apple. The people who work here have reinvented and defined entire industries with our products and services. The same dedication to innovation also applies to our approach to health - strengthening our commitment to leave the world better than we found it.
The Apple Health team is looking for a Clinical Specialist to support our cardiometabolic work. This is an outstanding opportunity for a clinician to demonstrate their medical expertise and passion to assist in building health focused technologies. In this role, you will partner with cross-disciplinary teams to identify key areas of focus with consideration for Apple’s products and technologies, define and develop new product concepts, and bring those concepts from idea to reality.
The ideal candidate will have a strong desire to innovate with a shown ability to execute, work closely with multi-functional teams, engage in open discussion, is consumer-focused, and does not shy from a challenge.
This is a site-based role.
As a Clinical Specialist, you play an integral role working with engineering and design teams to develop health focused products that impact heart health. Your key responsibilities include defining clinical features, designing clinical validation studies, and developing protocols for regulatory submissions. Your ability to articulate clearly with peers and leadership makes you a crucial team player, developing collaborative relationships with key partners across the Apple Health organization.
- Collaborate with design and engineering teams on clinical product development
- Craft detailed feature and set clinical specifications for heart-related products
- Support algorithm development including review of feasibility assessment studies
- Collaborate with regulatory and quality partners on product submissions to domestic/international regulators
- Communicate and maintain collaborative relationships - anticipate, adjust for, and communicate problems, risks, and roadblocks.
- Communicate clearly and concisely with peers, business partners, and leadership via the appropriate medium: verbal/written/presentation.
- MD/DO degree is required.
- Board Certified in Internal Medicine +/- subspecialty, Emergency Medicine, or Anesthesiology with an active US Medical License is a requirement.
- 1+ year(s) practicing as an attending.
- Health product and technology experience, preferably regulated medical products and/or digital health products.
- Strong communication and interpersonal skills with the ability to partner with a wide range of team members and experts.
- Experience in clinical development process for regulated health products, including clinical evidence generation, real world studies, working with observational data sets, and designing/executing pivotal clinical studies.