Relay Therapeutics Job Trends

The Director, Clinical Operations Excellence will establish and advance scalable, fit-for-purpose operational capabilities that enable high-quality, inspection-ready clinical trial execution across Relay’s portfolio, reporting to the VP, Clinical Operations Excellence. In a lean, matrixed biotechnology environment, this role will serve as both a strategic leader and hands-on contributor, partnering with study teams, functional stakeholders, CROs, and vendors to strengthen execution, simplify processes, develop actionable operational metrics and analytics, and proactively manage operational and quality risks. As the functional lead and business process owner for Risk-Based Quality Management (RBQM), this individual will be accountable for the implementation, adoption, and continuous improvement...

You will be an integral part of Relay’s drug product development team supporting Relay's research and development programs. You will be responsible for design and development of pre-clinical formulations to support discovery research and enable candidate selection/nomination. You will be responsible for collaborating with biology, medicinal chemistry, DMPK, and toxicology to execute scientific studies of discovery compounds in alignment with technical goals of the program You will be responsible for developing phase-appropriate oral drug product formulations and manufacturing process to enable early-stage clinical studies. Your Role You will lead and manage formulation development activities to support pre-clinical research and early...

The Opportunity As a member of our dynamic legal team, you will report to the Senior Director of Legal Operations and be directly responsible for implementation, maintenance and oversight of Relay Tx’s contract lifecycle management (CLM) platform and processes. You will be responsible for independently reviewing, drafting and negotiating contracts, overseeing the contract approval process, leading contract data integrity initiatives and implementing process improvements. You will lead end-to-end contract negotiation strategy and execution for a wide range of agreements such as master service agreements, software license agreements, consulting agreements, clinical trial agreements and additional agreements typical of the drug...

Are you a seasoned process chemist who enjoys working on drug substance projects? Do you love working closely with pharmaceutical development teams and external collaborators to seamlessly transition process development and help drug substance scale up and manufacturing efforts? In this role, you will be responsible for managing the chemical development and external manufacturing activities of our drug substance, you will have the opportunity to work across the various programs in our pipeline spanning from late research through clinical trials and beyond. Your Role You will support drug substance development efforts toward IND filing and continue to support the journey...

As a 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. Your Role Collaborate with senior medical staff, drug discovery teams, translational...

The Opportunity We are seeking an exceptional scientific leader to oversee our integrated Medicinal Chemistry, Computational Chemistry, Cheminformatics, and Drug Metabolism & Pharmacokinetics (DMPK) organizations. This individual willbe responsible fordriving the discovery and optimization of transformative small molecule therapeutics by building a highly collaborative, data-driven discovery engine that combines deep scientificexpertisewith modern computational approaches. The successful candidate will be a recognized leader in small molecule drug discovery with a proventrack recordof advancing programs from hit identification throughIND filing. Theywill be akey member of research leadership, fostering an environment where all disciplines work as a unified team torapidly...

You will be responsible for overseeing the supply chain operations for clinical trials, including the management of investigational medicinal products (IMPs) and comparators. This role will be pivotal in ensuring that study sites are supplied with the necessary products on time and in full compliance with regulatory requirements. The ideal candidate will have a strong analytical, organizational, and communication skill set, with the ability to manage multiple tasks in a dynamic, fast-paced environment. Your Role Monitor IP inventory levels at depots and clinical trial sites to proactively manage supply chain risks and prevent any interruptions to study timelines. Coordinate...