Global Medical Device & Life Sciences Policy Director

Oracle•United States,

15h•$114,600 - $234,600

About The Position

At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires policy leaders who are deeply steeped in the public and private levers that impact this industry. To remain competitive in this rapidly changing landscape, organizations require policy leaders who can navigate complex and fast-changing laws, regulations, and public policies across the globe. In this context, we are looking for a med-tech expert with experience in both SaMD and the use of AI in the life sciences industry to play a leadership role evaluating and influencing policy. This role will play a pivotal role in driving Oracle's success and competitiveness in the healthcare and life sciences sector. As Global Medical Device & Life Sciences Policy Director, you will lead regulatory policy efforts impacting our global AI-enabled, Cloud-native software applications used in clinical settings (Medical device and non-Medical Device) as well as our life sciences product offerings. We are seeking an experienced thought leader who is well respected and influential in the med-tech industry. You will establish strong partnerships with business teams to understand their products and policy needs as well as work cross functionally across the government affairs and legal and compliance group. You will track and evaluate regulatory developments impacting the company and lead our response to regulatory developments. You will also participate in trade association meetings and other thought leadership opportunities. The role is global in scope, but will involve collaboration with Medical Device and Life Sciences regulatory affairs, legal, and policy teams across the globe. We are seeking a leader who can keep up with the fast-paced environment of software development and an evolving regulatory landscape. Our team members are dedicated to excellence in their work, have instinctively good judgment and impeccable integrity. For this role we are seeking a leader who is strategic, collaborative, and a creative problem-solver.

Requirements

Med-tech expert with experience in both SaMD and the use of AI in the life sciences industry.
Well respected and influential in the med-tech industry.
Strategic, collaborative, and a creative problem-solver.
Ability to keep up with the fast-paced environment of software development and an evolving regulatory landscape.
Dedicated to excellence, with instinctively good judgment and impeccable integrity.

Responsibilities

Lead regulatory policy efforts impacting global AI-enabled, Cloud-native software applications used in clinical settings (Medical device and non-Medical Device) as well as life sciences product offerings.
Establish strong partnerships with business teams to understand their products and policy needs.
Work cross functionally across the government affairs and legal and compliance group.
Track and evaluate regulatory developments impacting the company and lead our response to regulatory developments.
Participate in trade association meetings and other thought leadership opportunities.
Collaborate with Medical Device and Life Sciences regulatory affairs, legal, and policy teams across the globe.