Full-Time

eTMF Specialist

Clinical Study Teams

Posted on 9/11/2025

Relay Therapeutics

Relay Therapeutics

201-500 employees

Drug discovery platform targeting protein motion

No salary listed

Cambridge, MA, USA

Remote

Category
Medical, Clinical & Veterinary (1)
Requirements
  • 2-5 years industry experience with TMF/eTMF
  • Hands-on experience with TMF QC processes, including both individual document quality checks and TMF completeness reviews
  • Working knowledge of ICH-GCP, FDA, and EMA regulations
  • Working knowledge of the CDISC TMF Reference Model
  • Veeva Vault eTMF experience a plus
  • Excellent organizational skills with the ability to multi-task and prioritize effectively in an extremely fast-paced and dynamic environment
  • Outstanding verbal and written communication skills
  • Strong work ethic, excellent problem-solving ability, and attention to detail and quality are critical to success
Responsibilities
  • Engage in assessing eTMF metrics for completeness, timeliness, and quality
  • Facilitate TMF QC Reviews and ensure issues identified are tracked to resolution
  • Help build and maintain strong partnership with key stakeholders to ensure cross-functional eTMF engagement
  • Engage with CROs/Vendors to ensure responsibilities around eTMF are clearly defined and executed
  • Contribute to eTMF study creation, maintenance, and archival, ensuring all activities are performed in accordance with Relay’s Standard Operating Procedures (SOPs), ICH-GCP Guidelines, EMA, FDA, and other health authority requirements
  • Apply risk-based quality management (RBQM) principles to Trial Master File (TMF) oversight, ensuring proportionate review, inspection readiness, and regulatory compliance
  • Help identify business needs to assess the current state of eTMF and identify opportunities for process improvement, ensuring industry best practice is implemented
  • Participate in the creation and review of Study-specific eTMF Plans, Study-specific TMF Indexes, and QC approach across all studies
  • Participate in discussions with IT and eTMF system managed services relations and topics
  • May participate in health authority inspections and audits
Desired Qualifications
  • Veeva Vault eTMF experience a plus

Relay Therapeutics uses its Dynamo platform to discover drugs by exploring how proteins move, enabling them to target proteins previously considered undruggable. The platform blends experimental data with computational modeling to identify and optimize therapeutic candidates, with a focus on precision oncology and genetic diseases. Its approach combines motion biology, data-driven design, and active partnerships (such as a worldwide license and collaboration with Genentech) with an internal drug pipeline. The company aims to bring life-changing medicines to patients by advancing clinical trials and securing licensing collaborations to fund and validate its therapies.

Company Size

201-500

Company Stage

IPO

Headquarters

Cambridge, Massachusetts

Founded

2016

Simplify Jobs

Simplify's Take

What believers are saying

  • Zovegalisib advances to Phase 3 ReDiscover-2 trial in HR+/HER2- breast cancer.
  • Nextech Invest buys $6.1M shares on February 17, 2026, amid 197% stock surge.
  • Three new preclinical programs disclosed June 6, 2024, expand Dynamo pipeline.

What critics are saying

  • Third layoffs cut 70 employees in nine months, delaying pipeline by 3-6 months.
  • Q1 2026 revenue miss prompts 12% analyst cut to $8.54M for 2026.
  • Cash burn forces dilutive offering at $12/share, risks Nasdaq delisting in 6-12 months.

What makes Relay Therapeutics unique

  • Dynamo platform discovers allosteric sites via protein motion simulations.
  • RLY-2608 is first pan-mutant PI3Kα inhibitor targeting H1047X, E542X, E545X.
  • REL-DEL integrates machine learning with DNA-encoded libraries for hit finding.

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Benefits

Medical, dental, vision

Life, disability, & FSA

401k

Commuter benefits

Parental leave

Home office stipend

Tuition reimbursement

PTO

Growth & Insights and Company News

Headcount

6 month growth

-2%

1 year growth

-9%

2 year growth

-3%
Yahoo Finance
Mar 19th, 2026
Nextech Invest bets $6M on Relay Therapeutics as shares surge 197% in a year

Nextech Invest purchased 855,097 additional shares of Relay Therapeutics for approximately $6.1 million, according to a Securities and Exchange Commission filing dated 17 February. The transaction brings Relay to 3.9% of Nextech's reportable assets under management. Relay Therapeutics, a clinical-stage biotech developing precision medicines for oncology and genetic diseases, has seen shares rise 197% over the past year to $9.93. The company currently has a market capitalisation of $1.77 billion with trailing revenue of $15.4 million. Nextech, a Switzerland-based investment firm specialising in concentrated bets on clinical-stage biotech companies, maintains Revolution Medicines as its largest holding at 58.5% of assets. Despite the purchase, Relay does not feature among Nextech's top-five holdings.

GlobeNewswire
Feb 4th, 2026
Relay Therapeutics to Participate in Guggenheim Emerging Outlook: Biotech Summit 2026

Relay Therapeutics to participate in Guggenheim Emerging Outlook: Biotech Summit 2026. CAMBRIDGE, Mass., Feb. 04, 2026 (GLOBE NEWSWIRE) - Relay Therapeutics, Inc. (Nasdaq: RLAY), a clinical-stage, small molecule precision medicine company developing potentially life-changing therapies for patients living with cancer and genetic disease, today announced that management will participate in a fireside chat at the Guggenheim Emerging Outlook: Biotech Summit 2026 on Wednesday, February 11, 2026 at 10:30 a.m. ET. The fireside chats will be webcast live and may be accessed through Relay Therapeutics' website under Events in the News & Events section through the following link: https://ir.relaytx.com/news-events/events-presentations. An archived replay of the webcast will be available for up to 30 days following the event. About Relay Therapeutics Relay Therapeutics (Nasdaq: RLAY) is a clinical-stage, small molecule precision medicine company developing potentially life-changing therapies for patients living with cancer and genetic disease. Relay's Dynamo(R) platform integrates an array of leading-edge computational and experimental approaches designed to drug protein targets that have previously been intractable or inadequately addressed. The company's lead clinical asset, zovegalisib, is the first pan-mutant selective PI3Kα inhibitor to enter clinical development and is currently in a Phase 3 clinical trial (ReDiscover-2) in HR+/HER2- metastatic breast cancer. Zovegalisib is also being investigated in a group of genetic disease indications called PI3Kα-driven vascular anomalies. Relay's pipeline also includes programs for NRAS-driven solid tumors and Fabry disease. For more information, please visit www.relaytx.com or follow us on LinkedIn.

Briefmobile
Oct 29th, 2025
AI in Drug Discovery Market Surges, Topping $15 Billion by 2032 as Top Players Forge New Frontiers

AI in Drug Discovery Market surges, topping $15 billion by 2032 as top players forge new frontiers. The race to revolutionize medicine is accelerating at a breakneck pace, not within the sterile confines of a traditional lab, but inside the complex algorithms of artificial intelligence. The field of AI in drug discovery, once a futuristic promise, is now a multi-billion-dollar engine of innovation, attracting colossal investments and strategic mergers as a cadre of top players vie for dominance. With the pharmaceutical industry grappling with soaring R&D costs and high failure rates, AI has emerged as the most potent tool to slash development timelines, reduce costs, and bring life-saving treatments to patients faster. The market's staggering potential is now quantified. The Artificial Intelligence in Drug Discovery Market was valued at USD 1.92 billion in 2024 and is expected to reach USD 15.50 billion by 2032, growing at a Compound Annual Growth Rate (CAGR) of 29.89% from 2025-2032. This explosive growth is fueled by a convergence of factors: an unprecedented flood of venture capital, a flurry of high-stakes partnerships between AI biotechs and pharmaceutical giants, and a pipeline of AI-discovered drugs now advancing through clinical trials, proving the technology's tangible value. The investment gold rush. Venture capital and corporate investment are the lifeblood of this nascent industry. In recent years, funding rounds have ballooned from millions to hundreds of millions, as investors bet big on AI's potential to disrupt the $1.5 trillion pharmaceutical market. "Investors are no longer just funding science projects; they are backing validated platforms that have demonstrated an ability to identify novel drug candidates with a higher probability of success," says Dr. Anya Sharma, a leading biotech analyst. "The capital influx is allowing these companies to move beyond software and build robust, integrated drug discovery and development engines." Companies like Exscientia, Recursion Pharmaceuticals, and Relay Therapeutics have collectively raised over $2 billion in funding, enabling them to build extensive pipelines. Exscientia, for instance, was the first to advance an AI-designed drug into human clinical trials and has since forged strategic collaborations with the likes of Sanofi and Bayer worth up to $6 billion in potential biobucks. Mergers, acquisitions, and the partnership paradigm. The landscape is also being reshaped by strategic consolidation. The "build vs. buy" dilemma is leading major pharmaceutical companies to either acquire promising AI startups outright or enter into massive, multi-year partnerships. In one of the most significant moves, Bristol Myers Squibb entered a deal potentially worth over $1.2 billion with Exscientia to discover small-molecule drug candidates in oncology and immunology. Similarly, Sanofi has pivoted aggressively towards AI, signing a $1.2 billion partnership with Atomwise to apply its AI-based atomistic technology to discover and develop up to five drug targets. "The M&A activity is a clear signal that Big Pharma views AI not as a niche tool, but as a core competency necessary for future survival," notes Michael Thorne, Chief Strategy Officer at a global consultancy firm. "We are witnessing the early stages of a land grab, where pharma giants are securing access to the most promising AI platforms to de-risk their R&D pipelines." Beyond partnerships, outright acquisitions are also on the table. NVIDIA, the chipmaker whose hardware powers much of the AI revolution, has made strategic investments in numerous AI biotechs, recognizing the sector's insatiable demand for computational power. This blurring of lines between tech and biotech underscores the deeply interdisciplinary nature of the modern drug discovery process. Top players and their divergent strategies. A clear hierarchy of top players is emerging, each with a distinct technological focus and business model. * Tech-Enabled Biotechs (e.g., Exscientia, Recursion, Relay Therapeutics): These companies use their proprietary AI platforms to discover and develop their own drug pipelines. Their value is tied directly to clinical success, making them high-risk, high-reward entities. Recursion, for example, has built one of the industry's largest proprietary biological and chemical datasets, which it uses to train its AI models for rapid phenotypic drug discovery. * AI Software and Service Providers (e.g., Schrödinger, Atomwise, BenevolentAI): These firms primarily operate a "platform-as-a-service" model, partnering with pharmaceutical companies to apply their AI tools for a fee, often including significant milestone and royalty payments. Schrödinger's physics-based computational platform is a industry standard for molecular modeling, used by nearly all major pharma companies. * Big Pharma In-House Efforts (e.g., AstraZeneca, Pfizer, Johnson & Johnson): Recognizing the strategic imperative, traditional pharmaceutical giants are building substantial internal AI and data science teams. AstraZeneca, for instance, has developed a robust AI-powered platform across its R&D spectrum, from target identification to clinical trial optimization. * Tech Giants (e.g., Google DeepMind, NVIDIA): With their vast computational resources and AI research prowess, tech giants are entering the fray. Google DeepMind's AlphaFold, which accurately predicts protein structures, has been hailed as a revolutionary breakthrough, providing a foundational dataset that accelerates target identification for the entire industry. Clinical validation: the ultimate proof. The critical question moving forward is clinical validation. While over 150 AI-discovered drugs are now in various stages of preclinical and clinical development, the field is eagerly awaiting its first fully AI-discovered drug to gain regulatory approval. Several candidates are showing promise. Exscientia's DSP-1181, a drug for obsessive-compulsive disorder discovered in just 12 months (compared to the industry average of 4-5 years), completed its Phase I trial. Insilico Medicine, another leader, recently dosed the first healthy volunteers in a Phase I trial for its AI-discovered drug for idiopathic pulmonary fibrosis, a project that took just 30 months from target discovery to candidate nomination. "Every successful clinical trial milestone achieved by an AI-discovered drug adds another layer of credibility to the entire sector," explains Dr. Sharma. "It moves the narrative from 'if' AI will work to 'how soon' and 'at what scale'." Challenges and the road ahead. Despite the euphoria, the path is not without obstacles. The "black box" nature of some complex AI models can make it difficult for researchers to understand why a specific molecule was chosen, posing challenges for regulatory review. Data quality and standardization remain a hurdle, as AI models are only as good as the data they are trained on. Furthermore, integrating these new, agile AI workflows into the traditionally slow and rigid pharmaceutical R&D process presents a significant cultural and operational challenge. Nevertheless, the momentum is undeniable. As algorithms become more sophisticated, datasets more expansive, and computational power more accessible, the impact of AI on drug discovery is set to deepen. The $15 billion market forecast is not just a number; it represents a fundamental shift in how humanity will combat disease in the 21st century. The top players of today are not only competing for market share - they are architecting the future of medicine itself.

ETF Daily News
Sep 8th, 2025
Ieq Capital LLC Makes New Investment in Relay Therapeutics, Inc. $RLAY

Ieq Capital LLC acquired a new position in shares of Relay Therapeutics, Inc. (NASDAQ:RLAY – Free Report) during the 1st quarter, Holdings Channel.com reports. The firm acquired 56,334 shares of the company’s stock, valued at approximately $148,000. Other hedge funds and other institutional investors have also bought and sold shares of the company. Allspring Global […]

Endpoints News
Apr 4th, 2025
Relay Therapeutics does third round of layoffs in nine months, affecting about 70 employees

Relay Therapeutics does third round of layoffs in nine months, affecting about 70 employees.

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