Commercial Relations - US

Reposted One Month Ago
4 Locations
In-Office or Remote
175K-250K Annually
Entry level
Healthtech • Software
The Role
The role involves building commercial relationships with regulatory consultants and industry stakeholders in the US digital health industry, enhancing Scarlet's presence in the market. Responsibilities include networking, knowledge sharing, attending events, and collaborating with the Commercial team to achieve goals.
Summary Generated by Built In

We pull medical technology from the future to solve human health.

 

Scarlet is authorised to assess and certify medical devices. We combine clinical, technical and regulatory expertise with AI agents and software so rigorous certification can keep pace with product development at the world’s most ambitious technology companies, without lowering the safety bar.

Our customers have cut a year or more from their certification timelines for new AI-enabled medical devices and shortened product-update cycles from months to weeks. You’ll join a team building the infrastructure that makes these outcomes repeatable at scale.

About the role

Be our first commercial hire in the US! Your goal is to build relationships with regulatory consultants, regulatory attorneys, and other key third parties, such that they advocate for Scarlet and recommend us to their clients in the right context. In practice this means building both knowledge (so they understand who we are and what makes us different) and trust (so they are confident in working with us).


Responsibilities
  • Build productive connections with individuals and organisations in Scarlet's ecosystem

  • Furnish these connections with the required knowledge and material to understand Scarlet and the value we offer to healthcare innovators.

  • Attend industry events to grow awareness and adoption of Scarlet

  • Collaborate closely with members of the Commercial team to effectively communicate Scarlet's mission and value proposition

  • Develop and iterate strategy and processes to align with our commercial goals.

Required qualifications
  • You have strong experience of developing a productive professional network and establishing commercial relationships with key industry stakeholders.

  • You're insatiably curious about the world and what makes people tick

  • You have a high EQ, hugely enjoy meeting people, and can easily navigate complex human relationships

  • You can build rapport with people across the industry: from senior figures at established firms to one-person consultancies, and everyone in between

  • You have exceptional written & verbal communication skills and you understand the importance of thoughtfully following up with the people you meet.

  • You balance thoughtful reflection with action; you can both think deeply and operate at pace

  • You are keen to travel up to 40% of the time

Preferred qualifications
  • You have a well-developed network in, and the knowledge of, the US digital health industry.

  • You are familiar with medical device regulation and Software as a Medical Device

 
Interview Process
  1. Intro call with Amnon - 20 mins

  2. Interview with Amnon - 45 mins

  3. Interview with someone else from the Commercial team - 30min

  4. Case interview with Dan - 1 hour

  5. Interview with Jamie - 30 mins

  6. Interview with James - 30 mins

  7. Referencing

  8. Offer

Skills Required

  • Experience in developing a professional network
  • Expertise in commercial relationships with industry stakeholders
  • Exceptional written and verbal communication skills
  • Ability to think deeply and act swiftly
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The Company
London
51 Employees
Year Founded: 2020

What We Do

Scarlet certifies software medical devices. We are Europe’s only Notified Body specialised in Software & AI. Our mission is to hasten the transition to accessible, affordable healthcare. We strive to achieve our mission by enabling our customers to deliver on theirs, and get their life-changing technology to the people who need it. Scarlet was built specifically for software and AI medical devices. We help customers to get their SaMD certified in the EU & UK, and ship the kind of regular updates inherent to good software, ensuring patients can safely get the most up-to-date technology. 

 Scarlet is designated as an EU Notified Body under regulation (EU) 2017/745 (EU MDR). And a UK Approved Body under UK Medical Devices Regulations 2002 (SI 2002/618 as amended). Scarlet is also accredited to issue ISO 13485 certificates

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