
EQRx is uniquely positioned to revolutionize how medicines are brought to patients through innovation and strategic collaboration across global healthcare systems—it’s an opportunity to make a real impact.
Michael Doherty Chief Regulatory Affairs
EQRx is uniquely positioned to revolutionize how medicines are brought to patients through innovation and strategic collaboration across global healthcare systems—it’s an opportunity to make a real impact.
Michael Doherty Chief Regulatory Affairs
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.
As Manager, Clinical Data Management you will lead the oversight of Clinical Data Management (CDM) activities for multiple clinical trials. This position will report to the Director of Clinical Data Management. You will ensure all Clinical Data Management (CDM) tasks and activities adhere to Good Clinical Practices to provide high quality data for analysis.
You will act as a Subject Matter Expert and be responsible for multiple studies. You will lead the execution of CDM tasks according to timelines and identify risks and mitigate as appropriate. You will lead all study specific CDM activities, including data review and reconciliation, User Acceptance Testing and study design. This role will also lead the filing of CDM documentation, ensuring expectations are met and providing oversight of the study level CDM TMF.
You will collaborate and lead with a cross functional team the development and review of CDM study level documentation, including the Data Management Plan, Data Review Plan, eCRF Completion Guidelines and Data Transfer Specifications. You will assist in the review of clinical study documentation including the study protocol and project timelines. You will generate and analyze CDM metrics, recognizing potential trends and issues and escalate as appropriate.
The Manager, Clinical Data Management will assist in the development of study timelines and prioritization of work to ensure that CDM tasks are delivered on time and with high quality. You will lead the planning and facilitation of CDM meetings and assess study and program risks, developing risk mitigation strategies and solutions.
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.
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.
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:
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.
*As EQRx grows, please note that some of these are subject to change.