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

We are seeking a Medical Writing Consultant with regulatory filing experience to be a dedicated resource as we build our organization. You will prepare, edit, and finalize clinical protocols, investigator brochures, synopses, regulatory documents and related clinical documents, such as abstracts, posters, presentations, manuscripts in addition to other core medical writing deliverables. You contribute to identifying key document messages and supporting data. You will partner with the study biostatistician to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings (TFLs), and narrative planning for relevant documents. You will work closely with the study team to ensure that results and messages in clinical documents accurately reflect the underlying data and key information sources. You will collaborate with clinicians, clinical scientists, biostatisticians, and pharmacokineticists to interpret study results and ensure study results and statistical interpretations are accurately and clearly reflected in relevant documents. You will manage the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed. You will ensure that appropriate documented quality control (QC) checks are performed on medical writing deliverables and work closely with the study team to reach consensus on timelines for deliverables.

The Impact You Will Have

• This is not your standard Medical Writing position. EQRx is on a mission to Remaking Medicine and this role is critical to our success. This position is a highly visible role that will help us drive forward towards our pinnacle goal of truly putting patients first.

Your Superpowers

• You have a Masters or PhD in a life-sciences field (e.g. Medical, Biology, Biochemistry, Molecular Biology or other relevant scientific or clinical discipline).
• You have advanced clinical regulatory document writing and review skills.
• You have a demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., International Council for Harmonisation and Good Clinical Practice.
• You have a strong interest and experience in exploring new technologies related to documentation and efficiency.
• You have a strong understanding of relevant scientific and medical terminology and statistical methods.
• You have experience with policy, guidance, and procedure development and maintenance.
• You have global experience and have driven new system adoption.
• You demonstrate the ability to analyze existing processes and implement effective changes as needed.
• You have Oncology and immuno-inflammatory experience.
• You can coordinate the ongoing evaluation of products technologies, services, and processes.
• You can identify opportunities to reduce costs and improve timelines.
• You are constantly reviewing publications and information sources to keep updated on current regulations, practices, procedures and proposals.
• You monitor industry best practices, changes in global regulations and guidelines and recommend changes and upgrades to existing policies, SOPs and systems.
• You have a working knowledge of International Council for Harmonisation and Good Clinical Practice guidelines and in-depth knowledge of clinical research processes, regulation and methodology.
• You can participate and work effectively on multiple cross-functional teams.
• You play well in the sandbox. 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.
• Job Code:

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.