Team Photograph: Photograph for ASSOCIATE DIRECTOR/ DIRECTOR, BIOANALYTICAL SCIENCES (BIOLOGICS)

We have a responsibility to build upon the incredible progress that has been made in understanding the biology of disease and to develop life-changing medicines that allow for sustainable, equitable access. We’ve seen success in other industry’s market-based, disruptive solutions - now is the time for healthcare.

Alexis Borisy Executive Chairman, Board of Directors

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.

What You’ll Do

You will work with the bioanalytical sciences team to support the bioanalytical and safety programs at EQRx to advance biotherapeutic products into the clinic, and to facilitate the development and approval/post-approval across all therapeutic areas. This team will work closely with internal and external stakeholders and streamline bioanalytical efforts with the appropriate level of expertise that is expected by program teams, functions and regulatory agencies.   

You will be responsible for biologics bioanalytical and immunogenicity assay development and validation, sample analyses, data interpretation and delivery of results and reports from early research programs right through to clinical trials. You’ll work closely with customer groups including translational research, nonclinical development, clinical pharmacology, and clinical development teams to define program preclinical and clinical assay specifications in support of program goals for biotherapeutic products. This person will enable and manage CRO provider vendor networks to develop and deliver relevant bioanalytical and immunogenicity assays to support PK/PD, translational clinical endpoints, biomarkers and diagnostics, and assure the highest quality of the data and adherence to the project timelines and budget.

You will ensure relevant GxP compliance, contribute to programs updates and appropriate sections of regulatory and other documents (e.g. nonclinical reports, clinical protocols, INDs, CTAs, BLAs, etc.). You’ll participate as a bioanalytical functional representative to program teams and play a major role in developing and maintaining a culture that is innovative, encourages risk, and supports the development of its people.

The Impact You Will Have

This is not your standard bioanalytical sciences position. We are doing things different here than how it is normally done, and this role is no exception. 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 have an MS or PhD degree in a relevant discipline with over 8 years of pharmaceutical or biotechnology experience or other relevant experience that includes a practical understanding of bioanalytical testing in support of research and development.
  • You are a subject matter expert in analytical techniques such as ligand-binding assays, flow cytometry, ELISA, ROA, and cell-based assays, etc.
  • You have technical expertise in critical reagent generation, immunogenicity assessment, cytokine profiling, companion diagnostics, genomic analysis, and other biomarker platforms.
  • You have demonstrated experience in bioanalytical methods, toxicology, and pharmacokinetic studies with a deep understanding of the development of the data packages to support nonclinical and clinical development.
  • You have in-depth experience with assay development/transfer/qualification/validation to external partners (CROs/CMOs) in a GLP/GxP environment.
  • You have hands-on experience preferably advancing biotherapeutic product(s) from phase I to approval and supporting post-marketing/commercial activities.
  • You have experience authoring bioanalytical sections of regulatory filings,especially modules 2.7.1 and 5.3.1.4.
  • Your scientific background and experience with cancer and cancer immunology is a plus.
  • You can work independently, analyze and work with attention to detail, process and prioritize sensitive complex information and problem solve.
  • You have strong interpersonal and communication skills, can participate, and work effectively on multiple cross-functional teams.
  • You can thrive in a smaller company environment and love the pace of a fast growing company.

 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.

Apply

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 Warrior

Are you ready to fight for enduring patient access?

  • Attribute Thumbnail: Leadership Leadership
  • Attribute Thumbnail: Problem Solving Problem Solving
  • Attribute Thumbnail: Efficiency Efficiency
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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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