Enveda Biosciences

Operations

• Translate complexity into clarity by distilling scientific, clinical, regulatory, and operational inputs into actionable insights and forward-leaning decisions.
• Own program execution end-to-end, identifying obstacles as efficiently as possible and doing whatever it takes to keep the program moving - whether that’s coordinating cross-functional dependencies, engaging with CRO partners, or designing dashboards that keep everyone aligned.
• Operate as a strategic thought partner to your Asset Entrepreneur, anticipating inflection points, modeling alternative scenarios, and helping to determine when to accelerate, pivot, or pause based on data and risk.
• Bring rigor and readiness to every forum, from Board updates to investor discussions, by delivering crisp data-driven slides, concise summaries, and decision-focused analyses.
• Maintain disciplined documentation and operational clarity, capturing key decisions, assumptions, and benchmarks while keeping dashboards, trackers, and updates accurate, accessible, and action-ready for asynchronous alignment.
• Contribute to Enveda’s institutional intelligence, documenting benchmarks, best practices, and learnings that make each future program faster and smarter.
• Your success will be measured not by the number of meetings you run, but by the speed, quality, and strategic depth of the asset’s decision-making and associated progress.

Program Strategy and Operations Director

Director

• Lead clinical pharmacology strategy across early- and late-stage clinical programs, including dose finding and exposure–response modeling.
• Oversee PK/PD study design, analysis, and interpretation, collaborating with clinical operations, biostatistics, and regulatory colleagues.
• Act as the subject-matter expert for clinical pharmacology in regulatory submissions and interactions with the FDA/EMA.

Director, Clinical Pharmacology

• Leverage your experience in Toxicology to successfully bring drugs from the bench to the clinic.
• Be part of the Non-Clinical Drug Safety (NCS) Team, reporting to the VP/Head of Nonclinical Drug Safety.
• Work cross-functionally in the Drug Development Team to contribute to our mission of expediting drug development to the clinic.
• Use your knowledge of Preclinical/Nonclinical Development, and all the FDA Guidance to Industry and ICH Regulatory Guidelines in support of Clinical Development.

Director, Toxicology

Business Development Rep

• Drive growth by sourcing, shaping, and negotiating partnerships, collaborations, and other business development opportunities aligned with Enveda’s strategy
• Oversee the full deal lifecycle, from triage and prioritization through diligence, negotiation, and close ensuring processes are efficient, rigorous, and decision-ready
• Lead preparations of data packages, analyses, and materials to support deal activities
• Guide partnering strategy in collaboration with key internal stakeholders
• Maintain a forward view of the market, integrating competitive intelligence, scientific trends, and partner feedback into actionable insights for leadership
• Represent Enveda at key conferences, investor meetings, and industry events
• Strengthen internal BD capabilities by building processes and systems
• Identify, negotiate, and execute strategic partnerships across Enveda’s discovery and development pipeline, translating science into collaborations with biotech, pharma, and other stakeholders

Vice President, Business Development

• Lead clinical development activities, including designing clinical studies and preparing regulatory documents | Provide clinical research summaries and collaborate with various departments to implement development programs | Offer clinical science insights into development programs and business development opportunities

Program Strategy and Operations Director

Director, Clinical Pharmacology

Director, Toxicology

Vice President, Business Development

Senior Director, Clinical Development