Director, Regulatory Affairs (CDx)

Do you have expertise in Companion Diagnostics, Clinical Trial Assays and Associated BioPharma Programmes, and bring a background in regulatory frameworks within Oncology or Rare Diseases? Do you want to be at the forefront of innovation, as we pioneer a movement to elevate standards of care globally, breaking barriers so health knows no limits?

If this sounds like you and you are driven by purpose, Join the SOPHiA GENETICS Regulatory Team as Director, Regulatory Affairs , and enable us to make a positive impact on the outcomes for cancer and rare disease patients worldwide.

Ideally, you will be in proximity to our Boston Fenway office, however suitably qualified candidates can be considered on a remote basis the US-North East. Due to high collaboration and team structure within Europe, this role wouldn't suit someone working remotely from the US West Coast.

Our Mission - BioPharma Solutions

Through a decentralized global network and patented algorithms, we give the BioPharma community access to high quality NGS solutions leveraging the SOPHiA DDM platform, including highly anticipated ctDNA-based solution in partnership with world-leading Academic Medical Center Memorial Sloan Kettering (MSK).

MSK ACCESS powered with SOPHiA DDM will be made available to BioPharma organisations to support R&D efforts, clinical trials and patients on a global scale.

Learn more about SOPHiA DDM BioPharma Solutions here :

Your Mission

Reporting directly to the EVP, Chief Legal & Regulatory Officer, this role works cross-functionally with internal teams, external BioPharma Partners and CROs to drive regulatory excellence

The vale you bring

• Provide strategic regulatory guidance for CDx collaborations with BioPharma partners, and work closely with the BioPharma business team on strategic initatives related to regulatory approvals and market access
• Drive efforts to secure regulatory designations and contribute to CDx strategy development and submissions
• Oversee and manage submissions for premarket approvals (PMAs), CTAs, IDEs, and other global regulatory filings.
• Represent SOPHiA GENETICS in regulatory meetings, including pre-submission meetings, advisory committees, and consultations with global health authorities.
• Provide regulatory intelligence, informed of evolving global regulatory landscapes, including changes in guidance related to IVD products, NGS, CDx, SaMD, and precision medicine.

Requirements

We know the every background is different, but to be best set for success we see you bringing :

As a public organisation facing ongoing commercial growth, you will bring a success-orientated and solutions-focused mindset that embraces team collaborations, change, growth and inclusion.

Benefits

You will be joining an organisation with the patient at the heart of every decision and action, driven by purpose as we pursue exponential growth.

Business recognition and accolades include :

Our US benefits package is comprehensive, but varies internationally in-line with local standards and laws. You can discuss a full breakdown with us, but as a brief overview :

Our DNA

Like the strands of DNA itself, SOPHiA GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient & Nimble and Fearlessly Adventurous

Our Virtues

At SOPHiA GENETICS we established our 7 Virtues to clarify how our principles show up each day through action. We Decide; We Do; We Collaborate; We Innovate; We Empower; We Adapt and We Learn.

At the centre of our Virtues is our Mantra, We Care, which provides a constant reminder of the compassionate, benevolent, and hopeful nature of our mission and how it should be threaded through each of our Virtues and everything we do. Learn more about our DNA and Virtues on our Careers portal

The process

We use the power of AI to help our partners make decisions. If you’re utilising AI in your search and application process, why not use some of these prompts :

Apply now with your CV and any supporting information.

Suitably qualified candidates will be invited through an interview and screening process where you will speak with members of our Talent Acquisition Team, the hiring leader alongside key colleagues and stakeholders from across the business. If you need additional support for accessibility, please contact our TA team for assistance.

We appreciate the value external partners can bring, but we operate a direct-hiring model and we are not looking to utilise agency support at this time. All hiring is controlled by Talent Acquisition, potential partners should liaise through TA and not our hiring teams please.

Starting Date : ASAP

Location : Boston, MA (Hybrid) or US North East Remote-Hybrid

Contract : Permanent