Enveda

• Design, build, and maintain scalable infrastructure for data engineering and analytics workloads in Databricks and Azure • Collaborate with data scientists, platform engineers, and DevOps to enable seamless integration between Databricks, data lakes, and other cloud services • Implement and manage CI/CD pipelines, infrastructure as code (Pulumi) and monitoring systems to support data platform operations • Drive improvements in security, observability, and automation for Azure and Databricks clusters, jobs, and user environments • Mentor junior engineers and contribute to infrastructure best practices, documentation, and internal tooling development

• Join Enveda as a CMC Director – Drug Product and help us transform natural compounds into life-changing medicines. • Play a key role in executing Enveda’s pharmaceutical development and manufacturing initiatives. • Guide CMC-related activities spanning oral solid dose drug product formulation development, manufacturing, and regulatory submissions. • Reporting directly to the VP, CMC, your contributions will be instrumental in executing our development and manufacturing strategies and ensuring the delivery of high-quality products to patients.

• Own the month-end, quarter-end, and year-end close process; ensure timeliness, accuracy, and GAAP compliance across all financial statements; maintain the general ledger, oversee journal entries, account reconciliations, and consolidations • Own complex areas critical to biotech including R&D and clinical trial expense accruals, stock-based compensation, leases, collaboration and licensing arrangements, revenue recognition, and equity/financing transactions; document positions in clear technical memos • Serve as the primary point of contact for external auditors; lead the annual financial statement audit from planning through issuance, including audit schedules, PBC requests, and management responses • Manage the company’s cash position, bank relationships, and investment accounts; oversee cash flow forecasting, wire approvals, and operating account controls; ensure clear visibility into the company’s liquidity runway at all times • Prepare accurate and timely internal financial reports (P&L, balance sheet, cash flow) for the CFO, executive team, and Board; design, implement, and maintain a robust internal control environment and accounting policies consistent with GAAP and SOX-readiness standards • Oversee federal, state, and local tax filings (or coordinate with external advisors); manage R&D tax credits and all regulatory reporting requirements • Evaluate, implement, and optimize accounting systems and finance tools (ERP, expense management, procurement workflows); deploy AI strategically and responsibly; scale and modernize the finance tech stack to meet the demands of a growing clinical-stage biotech • Manage relationships with external auditors, tax advisors, payroll providers, and accounting consultants; hold vendors accountable to scope, budget, and timeline • Directly manage, develop, and retain the finance team; serve as the day-to-day mentor and primary resource for finance staff; build a high-performance culture within the function

• Create the marketing strategy from the ground up for a new product • Write and publish social media copy across LinkedIn, X/Twitter, Instagram, YouTube, and more • Support paid social and digital ad campaigns - copy, targeting inputs, and performance monitoring • Contribute to performance dashboards (Google Analytics and paid platform reporting) and synthesize findings into actionable reporting • Coordinate with designers on visual assets to ensure consistency with brand guidelines • Support distribution of key corporate moments: pipeline updates, data readouts, press coverage, and conference appearances • Help maintain a content repurposing workflow so strong work gets the reach it deserves

• Manage customer service operations end-to-end: escalation pathways, response quality, tooling, and metrics • Partner with engineering and product to translate operational needs into clear, well-scoped software tickets • Work with marketing on campaign operations, launch logistics, and user acquisition workflows • Interface with external service partners on onboarding, coordination, and ongoing relationship management • Build dashboards and track KPIs to surface operational insights to leadership • Serve as the primary liaison between internal teams and external partners including legal counsel, third-party vendors, marketing, and customer service • Build the systems, playbooks, and processes that let the organization scale

• Lead DMPK and PK/PD strategy across discovery and development programs, from candidate nomination through clinical development and regulatory submission • Drive clinical pharmacology strategy including dose finding, exposure–response modeling, PK/PD analysis, and risk-benefit assessment for early- and late-stage programs • Oversee PK/PD study design, analysis, and interpretation, collaborating with clinical operations, biostatistics, and regulatory colleagues • Provide scientific and regulatory support for DMPK, Clinical Pharmacology, and Biopharmaceutics sections of regulatory submissions, including IND, NDA, and BLA filings • Act as the subject-matter expert for clinical pharmacology and DMPK in interactions with FDA, EMA, and other global health authorities • Partner with translational, discovery, and clinical teams to integrate nonclinical ADME data into clinical development plans and support compound progression from pipeline to early development • Work closely with Discovery and DMPK groups to provide PK/ADME support for discovery projects, enabling informed compound selection and optimization • Ensure alignment of DMPK and PK/PD activities with clinical development, drug manufacturing, and regulatory plans across the portfolio • Provide strategic and technical leadership to the AQP function on scientific matters, combining full-time and consulting resources • Plan and conduct stage-appropriate Clinical Pharmacology studies (Phase I/II/III) to support regulatory submissions

• Define and execute global regulatory strategies across early- and late-stage development for small molecules and combination products • Lead and oversee interactions with FDA, EMA, and other global regulatory agencies • Author, review, and submit key regulatory documents, including INDs, CTAs, briefing books, and response packages • Build and manage a high-performing regulatory team across strategy, operations, and publishing

• Distill scientific, clinical, regulatory, and operational inputs into clear insights and decisions for the C-suite • Own program execution end-to-end - removing blockers, coordinating cross-functional dependencies, and keeping CRO partnerships and dashboards on track • Serve as a strategic thought partner to the Asset Entrepreneur: anticipate inflection points, model scenarios, and help determine when to accelerate, pivot, or pause • Bring rigor to every forum - Board updates, investor and BD discussions - with crisp slides, concise summaries, and decision-focused analyses • Partner with functional experts across clinical, translational, regulatory, and CMC to integrate science and execution seamlessly • Leverage AI and digital tools to organize complexity, accelerate workflows, and sharpen decision-making • Contribute to Enveda's institutional intelligence by documenting benchmarks, best practices, and learnings that make future programs faster and smarter

• 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