Employer profile
Relay Therapeutics Inc
5 open roles indexed with location, benefit, and apply-link signals where available.
Open roles
Showing the most recent indexed roles for this employer.
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Executive Assistant
Cambridge, MA
unspecified $101K-$144KExecutive Assistant Cambridge, MA The Opportunity: We're looking for an Executive Assistant who takes pride in doing great work, cares deeply about helping others succeed, and is eager to learn how a business really runs. This role is about trust, follow-through, and showing up every day with a mindset of “How can I make things better?” You do not need prior biotech or corporate experience to succeed here. Some of the strongest candidates come from retail, hospitality, or customer-facing roles, where attention to detail, resilience, and clear communication are essential. If you've ever managed competing priorities during a busy shift, anticipated what someone needed before they asked, or taken pride in creating a great experience for others-you already have skills that translate well to this role. This is a fully in-office position, five days per week . Our culture is built on collaboration, shared lunches, and day-to-day camaraderie, and we believe being together in person makes us better teammates. Your Role: As an Executive Assistant, you'll be a key partner to senior leadership and an essential part of keeping things running smoothly. Your responsibilities will include: - Managing calendars, scheduling meetings, and keeping priorities organized - Handling email and communications with professionalism and discretion - Preparing documents, notes, and follow-ups so nothing falls through the cracks - Coordinating logistics for meetings, travel, and projects - Acting as a thoughtful point of contact for internal and external stakeholders - Anticipating needs and proactively solving problems before they become urgent - Learning
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Senior Manager, Drug Product
Cambridge, MA
unspecified $122K-$174KSenior Manager, Drug Product Cambridge, MA The Opportunity: - You will be an integral part of Relay's drug product development team supporting Relay's development programs. - You will be responsible for design and development of robust, scalable drug product formulation and manufacturing processes that ensure product quality and are commercially viable. - You will be overseeing technical activities at drug product CMOs, including technology transfer, clinical trial material (CTM) production, process troubleshooting, QbD and PAR studies, risk assessments, registration batch production, and process validation Your Role: - You will manage requisite formulation and process development (R&D) activities to support clinical development Relay pipeline programs. - You will be responsible for assessing and selecting appropriate packaging (container closure systems) for Relay's development products. - You will design and develop robust R&D and GMP stability studies for investigational drug products in collaboration with internal AD/QC team and third parties. - You will contribute to completion (author/review) of relevant drug product sections of regulatory submission documents (IND, IMPD, NDA, briefing packages etc.), responses to regulatory questions and supporting documentation in timely manner. - You will coordinate with analytical, quality and supply chain teams to ensure timely manufacture and release of drug product batches by leading technical reviews of batch records, deviations, change controls, and nonconformance investigations; proactively identify and mitigate risks related to clinical supply. - You will partner with drug substance and analytical development functions to define optimal drug substance properties and control strategies. - You will provide person-in-plant support for drug
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Scientist II, Cheminformatics
Cambridge, MA
hybrid $88K-$126KScientist II, Cheminformatics Cambridge, MA The Opportunity: Relay Therapeutics is seeking a highly motivated Scientist to join our Drug Discovery team in a unique hybrid role that integrates synthetic chemistry with cheminformatics. This position is ideal for a scientist who enjoys working at the interface of experimental and computational disciplines and is excited to help shape how data-driven chemistry is done in a modern biotech environment. Your Role: - Maintain and support tools used in compound registration, lab operations and data ingestion from assays, as well as broader data and software access workflows - Design and execute synthetic chemistry workflows, with a focus on high-throughput or parallel synthesis to support medicinal chemistry programs - Contribute to the design, enumeration, and prioritization of compound libraries using cheminformatics tools - Collaborate closely with computational chemists, data scientists, and medicinal chemists to guide compound design using data-driven insights - Analyze and interpret experimental data to inform structure-activity relationships (SAR) and compound optimization - Help develop and refine internal workflows that integrate synthetic chemistry with computational approaches - Maintain clear documentation and communicate results effectively across multidisciplinary teams Your Background: - Ph.D. or M.S. in Organic Chemistry or a related field, with 2-5 years of relevant industry experience preferred - Demonstrated experience in synthetic organic chemistry - Familiarity with cheminformatics tools and concepts (e.g., molecular representations, library design, property prediction) - Experience with scripting or data analysis tools (e.g., Python, RDKit) - Strong problem-solving skills and the ability to work both independently and collaboratively
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Associate Director, CMC Regulatory
Cambridge, MA
unspecified $145K-$207KAssociate Director, CMC Regulatory Cambridge, MA The Opportunity: As part of the Pharmaceutical Development team, this position will play a key role in regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) programs. Your Role: - You will serve as CMC-regulatory lead for assigned projects. - Develop and execute CMC global submission plans and timelines in accordance with project goals - You will lead the preparation/plans, review, and on-time submission of CMC sections for IND/IMPD/CTA, NDA/MAA and other global regulatory filings including IB, DSUR, annual updates, briefing books etc. in conjunction with regulatory affairs and CMC/Pharmaceutical Development leads/SMEs. - You will be responsible for coordination of responses to CMC questions/RFIs from regulatory authorities in conjunction with CMC and regulatory affairs leads/SMEs. - You will lead CMC-regulatory activities listed above with cross-functional teams and act as the regulatory CMC liaison between CMC/PD, regulatory affairs and/or program management, as applicable. - You will lead and manage CMC-regulatory assessment and guidance on product compliance topics, including change controls, deviations, and GMP investigations, in conjunction and consultation with CMC leadership. - You will keep abreast of regulatory guidance and technical/scientific developments relevant to projects. Competencies: - Strong background in Regulatory Affairs-CMC with a focus on small molecule clinical (IND/IMPD) and/or commercial (NDA/MAA) submissions. - Proven ability to lead and manage regulatory CMC projects with minimal supervision - In-depth knowledge of global CMC regulatory requirements and guidelines (e.g. FDA, EMA, ICH). - Positive attitude, energetic and proactive. - Strong technical writing and
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Senior / Medical Director
Cambridge, MA
unspecified $213K-$350KSenior / Medical Director Cambridge, MA The Opportunity: As a Senior / Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and execution. Working cross-functionally with clinical project management, regulatory affairs, clinical operations, biostatistics, data management and medical writing, you will play a key role as Relay Tx continues to introduce product candidates into the clinic. You will provide clinical leadership to R&D teams and will work closely with Development leadership. We are open to remote employees About You: - Collaborate with senior medical staff, drug discovery teams, translational oncology, clinical operations, clinical investigators and disease-specific experts to design and execute early clinical development plans that definitively test key translational hypotheses for Relay Tx medicines and establish clinical proof-of-concept as soon as possible after entering human testing. - Write clinical sections of key documents, including Investigator's Brochures, IND summary documents, CTAs for initiation of ex-US studies and work with senior medical staff for responses to questions from regulatory authorities, IRBs, and ethics committees. - Provide expert medical review, assessment, and interpretation of clinical data and prepare results for presentation to internal clinical development leadership and external stakeholder including regulatory authorities. - Manage drug safety and pharmacovigilance activities for ongoing trial(s). - Attend and support clinical site initiation visits. - Rapidly integrate new insights derived from on-going Relay Tx or external clinical trials, translational science