Enveda

• Maintain and continuously improve Enveda’s core financial models, including monthly forecasts, rolling budget updates, scenario analyses, and related reporting • Partner with cross-functional teams to translate scientific and operational inputs into clear financial implications, ensuring models accurately reflect business dynamics, scientific roadmaps, and operational priorities • Support quarterly close in close partnership with Accounting, including variance analysis, accruals, and financial reviews • Build and maintain reporting frameworks, dashboards, and metrics that provide visibility into R&D spend, portfolio progression, operational efficiency, and capital allocation • Prepare high-quality materials for Board meetings, investors, and executive leadership in partnership with the Director and VP of FP&A and CFO • Identify and implement opportunities to improve forecasting accuracy, streamline financial processes, and strengthen internal controls

• Lead end-to-end biosample and biomarker operations for Phase 1 SAD/MAD and Phase 2 clinical studies, as well as earlier-stage translational work • Develop biomarker sampling schemas, protocol sections, lab manuals, and kit specifications in collaboration with Translational Medicine and Clinical Operations • Coordinate biomarker assay development, validation, and sample management activities, involving all relevant internal and external stakeholders and ensuring technical feasibility • Manage end-to-end biospecimen lifecycle: sample collection, site training, shipment logistics, processing, and data transfer between internal teams and external partners • Partner with leaders and scientists across translational science, biology, clinical development, and CRO/vendor organizations to plan and execute biomarker operations • Serve as the primary liaison with CROs for study design, execution, and reporting; monitor data quality and deliver concise, actionable readouts to internal teams • Select and oversee central and specialty biomarker labs, managing vendor contracting, SOWs, POs, timelines, and data deliverable milestones • Manage CRO and vendor relationships for biomarker assay outsourcing, sample logistics, and translational study execution • Partner with Data Management to ensure clean, reconciled, analysis-ready biomarker datasets are delivered on time to support dose selection, mechanism validation, and study design decisions • Implement and optimize tracking systems and LIMS tools to manage workflows, sample inventory, and operational exceptions • Develop reusable SOPs, tracking tools, and reconciliation workflows to scale operations across the portfolio • Create dashboards and reports for communication of biomarker study progress, sample inventory, and assay timelines • Clearly communicate the status of projects, challenges, results, and proposed paths forward across internal and external stakeholders, teams, and time zones • Lead timelines and deliverables across multiple R&D programs spanning early discovery through clinical development • Turn scientific and commercial goals into clear, testable plans with explicit decision gates • Proactively manage risks and maintain tight coordination across R&D, CMC, and external partners • Ensure tasks and projects are delivered on-time, within scope and within budget through constant communication and follow-up with stakeholders • Assist Project Leaders in meeting management through agenda planning, providing status updates, and following up on action items • Explore opportunities for accelerating timelines and ensure resource availability and allocation

• Lead translational immunology strategy and execution for one of our lead assets in the clinic, focusing on biomarker development, translational plans, and scientific leadership of a novel best-in-disease mechanism • Act as a scientific bridge between discovery and clinical development teams, collaborating closely with preclinical, clinical, and operational leads • Build and maintain strong CRO relationships that enable the rapid turnaround needed to react to clinical observations • Translate emerging data into clear, actionable narratives for asset teams, leadership, and external audiences - with the speed and intellectual honesty the business demands • Serve as a core member of the asset team, partnering closely with MOATID on mechanistic hypotheses, Clinical Development on protocol design, and Clinical Operations on sample collection logistics and site feasibility

• Review, verify, and process vendor invoices for accuracy and proper authorization; match to purchase orders and resolve discrepancies promptly • Prepare and process electronic payments (ACH, wire transfers, checks) and monitor invoices to ensure timely disbursement • Maintain vendor records, support onboarding and banking coordination, and ensure compliance with required documentation • Build and maintain positive relationships with vendors and internal teams, addressing inquiries from stakeholders • Assist with AP subledger reconciliation, accrual preparation, and period close reporting • Partner with Procurement, Operations, and Budget Owners to resolve discrepancies and enforce AP policies • Ensure compliance with financial regulations, tax requirements (including 1099 reporting), and support internal and external audits • Support internal controls and participate in enhancements to AP workflows and automation as Enveda scales NetSuite

Let’s build the future of medicine - together. Join Enveda as a Sr. Director, Biomarker Operations & Translational Medicine in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference? Remote | Full-Time | $270,000-$300,000 What Makes Us Enveda Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait. What sets Enveda apart isn’t just what we do - it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day. Our Momentum - Unicorn status: Achieved following a $150 million Series D funding round in 2025 - Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024 - Award-winning culture: --Newsweek: Top 100 Global #MostLovedWorkplaces (2025) --Forbes: America’s Best Startup Employers (2024 & 2025) --Newsweek: America’s Greatest Startup Workplaces (2025) --LinkedIn: Top Startups to Watch (2024) These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a Sr. Director, Biomarker Operations & Translational Medicine, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in biomarker operations and translational medicine will be critical in accelerating our mission to transform natural compounds into effective treatments because every breakthrough starts with bold questions and brave actions. What You’ll Do - Lead biomarker strategy across ENV-294, ENV-308, ENV-6946, and ENV-096, supporting Phase 1 and Phase 2 study planning including biomarker-heavy trial design and execution - Partner with Translational Medicine to ensure biosample plans are fit-for-purpose for mechanism validation and decision-making, and collaborate with Clinical Operations on lab manuals, site workflows, sample logistics, and shipment processes - Work closely with Data Management to ensure datasets are complete, reconciled, and analysis- and submission-ready, while maintaining GCP/GLP/GCLP compliance and inspection readiness alongside Regulatory and Quality teams - Own selection, contracting, and strategic oversight of central and specialty labs across PK, ADA, exploratory biomarkers, omics, and imaging - including vendor governance, performance oversight, and cross-program portfolio optimization - Drive implementation of technology-enabled solutions including LIMS, vSIM, sample tracking, and inventory systems, while harmonizing SOPs and biospecimen best practices across programs - Lead workforce prioritization, workload balancing, and cross-program process alignment We're Looking For - A biomarker operations leader who has built or scaled functions across multiple clinical programs, comfortable owning cross-program standards while ensuring right sample, right processing, right vendor, right time execution - A strong people leader with experience building and managing teams of Biomarker Operations Managers, with deep expertise in biospecimen collection, processing, storage, tracking, destruction, and chain-of-custody rigor - A vendor-savvy professional experienced in selecting and governing central and specialty labs, with fluency in GCP/GLP/GCLP and audit readiness expectations - A systems thinker and proactive risk manager who anticipates operational failure points such as sample loss, delays, and protocol deviations and understands that technology amplifies strong processes but requires accountable ownership - Someone energized by high-growth, multi-asset environments where operational complexity increases rapidly If you’re passionate about innovation and impact, we encourage you to apply even if you don’t meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance Enveda is protecting Job Seekers: We care deeply about creating a safe, respectful experience for every applicant, so we wanted to share a few guidelines to help you spot anything that doesn’t feel right. --You’ll always meet real Enveda team members through video or in-person conversations before receiving an offer. --All communication from us will come from an @enveda.com or @envedabio.com email address. --We’ll never ask you to purchase equipment, send money, or share sensitive banking details as part of any step in our recruiting process. If something feels off or you’re unsure whether a message is truly from Enveda, please reach out at anytime at recruiting@enveda.com. At Enveda, we’re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.

Let’s build the future of medicine - together. Join Enveda as a Clinical Trial Associate in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference? Remote | Full-Time | $75,000 - $90,000 What Makes Us Enveda Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait. What sets Enveda apart isn’t just what we do - it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day. Our Momentum - Unicorn status: Achieved following a $150 million Series D funding round in 2025 - Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024 - Award-winning culture: Newsweek: Top 100 Global #MostLovedWorkplaces (2025) Forbes: America’s Best Startup Employers (2024 & 2025) Newsweek: America’s Greatest Startup Workplaces (2025) LinkedIn: Top Startups to Watch (2024) These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a Clinical Trial Associate, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to bring innovative treatments to market because every breakthrough starts with bold questions and brave actions. What You’ll Do - Support Clinical Trial Manager(s) in the day-to-day execution of one or more clinical trials, helping drive operational efficiency across the team - Coordinate and schedule meetings, compile materials, oversee presentations, and take and distribute accurate meeting minutes for internal and external stakeholders - Manage the Trial Master File and internal study files, ensuring Clinical Operations documentation is properly filed, routed, and maintained - Create, distribute, and maintain trackers for metric reporting, and prepare reports and requests as needed - File and route agreements and other documents related to Clinical Operations and Clinical Development - Contribute to departmental initiatives and process improvements - Minimal travel required (10% both international/domestic) We’re Looking For - B.S./B.A. degree required; science or healthcare-related fields preferred but not required - 3+ years of relevant professional experience, ideally within biotech, pharmaceutical, or medical device industries - Strong organizational and time management skills, with the ability to manage multiple priorities across one or more studies simultaneously - Excellent written and verbal communication skills, with proficiency in Microsoft Suite and Slack - Experience maintaining and managing study or program trackers, with a working knowledge of ICH/GCP guidelines and local regulations If you’re passionate about innovation and impact, we encourage you to apply even if you don’t meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance Enveda is protecting Job Seekers: We care deeply about creating a safe, respectful experience for every applicant, so we wanted to share a few guidelines to help you spot anything that doesn’t feel right. --You’ll always meet real Enveda team members through video or in-person conversations before receiving an offer. --All communication from us will come from an @enveda.com or @envedabio.com email address. --We’ll never ask you to purchase equipment, send money, or share sensitive banking details as part of any step in our recruiting process. If something feels off or you’re unsure whether a message is truly from Enveda, please reach out at anytime at recruiting@enveda.com. At Enveda, we’re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.

Let’s build the future of medicine - together. Join Enveda as a Senior Clinical Trial Manager in a remote capacity and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference? Remote | Full-Time | $155,000 - $170,000 What Makes Us Enveda Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait. What sets Enveda apart isn’t just what we do - it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day. Our Momentum - Unicorn status: Achieved following a $150 million Series D funding round in 2025 - Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024 - Award-winning culture: --Newsweek: Top 100 Global #MostLovedWorkplaces (2025) --Forbes: America’s Best Startup Employers (2024 & 2025) --Newsweek: America’s Greatest Startup Workplaces (2025) --LinkedIn: Top Startups to Watch (2024) These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a Senior Clinical Trial Manager, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in clinical trial management will be critical in accelerating our mission to innovate drug discovery because every breakthrough starts with bold questions and brave actions. What You’ll Do - Lead cross-functional trial teams to plan, execute, and deliver clinical trials in alignment with the development strategy, budget, and timeline - Oversee CRO and vendor selection, management, and performance - including leading bid-defense processes, contracts, change orders, and quality oversight - Author and review trial documents, SOPs, CRFs, and completion guidelines for internal and external use - Conduct hands-on clinical monitoring for early phase trials (SQV, SIV, IMV, COV), including report writing, review, and approval - Manage trial budgets, triage issues to leadership, and maintain dashboards and status reports on timelines, accruals, and risks - Serve as a subject matter expert during regulatory inspections and contribute to departmental process improvements - Up to 30% domestic and/or international travel We’re Looking For - B.S./B.A. degree preferred, with 10+ years of experience in a pharmaceutical, biotech, or CRO environment - 5+ years managing clinical trials, including CRO management and oversight in early phase studies - 2+ years in a CRA role with direct clinical monitoring experience - Experience leading the bid-defense process for CRO selection, with a strong grasp of regulatory requirements and ICH/GCP guidelines governing global clinical research - Proven ability to manage competing priorities, meet deadlines, and escalate issues in a timely manner, with excellent written and verbal communication skills - Proficiency in Microsoft Suite and clinical project management tools, with experience executing trials across multiple countries and regions If you’re passionate about innovation and impact, we encourage you to apply even if you don’t meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance Enveda is protecting Job Seekers: We care deeply about creating a safe, respectful experience for every applicant, so we wanted to share a few guidelines to help you spot anything that doesn’t feel right. --You’ll always meet real Enveda team members through video or in-person conversations before receiving an offer. --All communication from us will come from an @enveda.com or @envedabio.com email address. --We’ll never ask you to purchase equipment, send money, or share sensitive banking details as part of any step in our recruiting process. If something feels off or you’re unsure whether a message is truly from Enveda, please reach out at anytime at recruiting@enveda.com. At Enveda, we’re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.