Team Photograph: Photograph for Pharmacovigilance Medical Director

Across the healthcare continuum, there is a shared common concern regarding rising drug spend and drug pricing. EQRx’s innovative business model addresses the profound need for a more collaborative approach across the ecosystem to solve the challenges of patient access to innovative medicine at radically lower prices.

Kent Rogers Chief Customer Officer

EQRx believes responsibility can be revolutionary. Want to make a difference while advancing your career? Come join a team that is working towards our bold mission of developing innovative medicines at radically low prices to help people get the medicines they need.

EQRx believes responsibility can be revolutionary. Want to make a difference while advancing your career? Come join a team that is working towards our bold mission of developing innovative medicines at radically low prices to help people get the medicines they need.

Who We Are

We're a new kind of biotech, one with a bold mission to bring innovative new medicines at dramatically lower costs.

What You’ll Do

You will act as the global safety lead for assigned pre- and/or post-marketing compounds. This role will lead the safety activities and benefit-risk strategies for assigned EQRx compound(s)/ programs and chair/co-chair the product SMT(s). You will lead the medical safety oversight of and execution of risk management strategies and RMP elements for assigned products and responses to HA queries. You will ensure ongoing and adequate safety surveillance and timely detection and communication of new safety issues.

You will provide safety input to safety-related documents, including but not limited to clinical development plans, study protocols, amendments, IB, statistical analysis plan (SAP), ICF, CSR, approve safety aggregate reports, product renewal submissions, and post-marketing study documents and reports. You will provide safety lead support for global submission document production, including integrated safety data review, integrated safety summary document review, and safety-focused publication development. This role will oversee, prepare, and review aggregate safety review documents (e.g., DSUR, PBRER) and safety sections of relevant clinical trial documents (e.g., protocols, clinical study report [CSR], investigator brochure [IB], informed consent form [ICF]) and regulatory filings (e.g., clinical trial applications [CTA], marketing authorization applications [MAA]). You will also support the EU QPPV or other regional or local Qualified Person for PV relative to issues relating to assigned products.

The Impact You Will Have

This is not your standard PV role. This position is highly visible and of significant impact to the company. We are on a critical mission to bring quality solutions to patients at a fraction of the price. This role will help us drive forward towards that pinnacle goal of truly putting patients first.    

 

Your Superpowers

You are an MD.

You have at least 3+ years of extensive relevant pharmaceutical industry experience in the safety and risk management area - including in signal detection, validation, and management.

You have oncology drug safety experience (clinical experience preferred).

You are a results-driven leader who drives teams to foster a proactive solution-oriented to safety signal detection, evaluation, and risk management.

You have a very thorough knowledge and understanding of PV deliverables, standards, and processes at a global level, including pre and post-launch experience.

You have NDA/BLA experience.

You have excellent interpersonal, analytical, managerial, and organizational skills.

You can participate and work effectively on multiple cross-functional teams

You understand relationships are key and have strong interpersonal skills.

You are a leader. Teams love working with you and you are someone who takes pride in mentoring and supporting the careers of others.

You can thrive in a smaller company environment and love the pace of a true startup

You’re a team player who is willing to roll-up your sleeves and get the job done.

Are you bold enough?

Your work should matter and allow you the freedom to be 100% you. We spend too much time and effort in our career to not feel excited and proud about what we do and who we do it with. In other words, your career is too important for your next move to be just another job, so let’s work together to change the world and bring affordable medicines to all patients.

We aren’t about a bunch of empty slogans on a wall or words on a coffee cup – you can find that in lots of places. We are a culture of individuals with diverse backgrounds and personalities. What does EQRx stand for? 

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Are you bold enough?

Your work should matter and allow you the freedom to be 100% you. We spend too much time and effort in our career to not feel excited and proud about what we do and who we do it with. In other words, your career is too important for your next move to be just another job, so let’s work together to change the world and bring affordable medicines to all patients.

We aren’t about a bunch of empty slogans on a wall or words on a coffee cup – you can find that in lots of places. We are a culture of individuals with diverse backgrounds and personalities.

The Disruptor

Are you ready to make waves in the industry and change the tides?

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What does EQRx stand for?

  • EQuality Medicines: Equally good or better, innovative medicines
  • EQuitable Medicines: Making innovative medicines affordable
  • EQual Access: Sustainable, frictionless access for people to cutting-edge medicines

We have a bold mission and are looking for equally bold people who want to join us and help make a difference in the world. If you want to grease the wheel we are definitely not for you. Want to build the wheel? We might be just what you are looking for.

EQRx is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

It’s (mutually) beneficial.

You’re curious about what sets us apart from the rest. What do you get from working at EQRx?

So, let’s start big—working at EQRx means having the opportunity to change the world.

By joining a team that’s remaking medicine development from start to finish, you’re going to enjoy the daily rush of throwing caution to the wind and doing things differently by:

  • Working with the smartest game-changers in the industry
  • Cutting down the red tape of “the way things are done”
  • Seeing and feeling the daily impact of your work
  • Growing as a professional and a person
  • Committing to neverending social responsibility

And, yes—we also have a killer list of things that’ll help you shine as part of the team.

But to us, these are just table stakes.

  • 100% Medical, Dental, and Vision coverage
  • Flexible Spending Account
  • Health Reimbursement Account
  • Free snacks and drinks

*As EQRx grows, please note that some of these are subject to change.

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