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Recursion Announces Vicki Goodman, M.D., as Incoming Chief Medical Officer

(Neutral)
(Very Positive)
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Recursion (Nasdaq: RXRX) named Vicki Goodman, M.D. as Chief Medical Officer effective April 6, 2026, succeeding David Mauro, M.D., Ph.D., who will transition from the role after approximately three years.

Recursion highlighted Dr. Goodman’s late‑stage oncology and regulatory experience as supportive for advancing its clinical pipeline, including ongoing progression of REC‑4881.

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Positive

  • Experienced CMO hire effective April 6, 2026
  • Late‑stage oncology and FDA reviewer expertise
  • Continued progression of REC‑4881

Negative

  • CMO transition with David Mauro leaving after approximately three years

Market Context

This announcement highlights a senior leadership transition as Vicki Goodman, M.D., prepares to assu...
Analysis

This announcement highlights a senior leadership transition as Vicki Goodman, M.D., prepares to assume the CMO role on April 6, 2026. Her background spans oncology development, FDA service, and major pharma portfolios, aligning with Recursion’s stated focus on late-stage clinical and regulatory milestones. In context of recent earnings strength and active financing tools, investors may watch how her leadership influences trial progress and regulatory interactions across the pipeline.

Key Figures

CMO start date: April 6, 2026 Current CMO tenure: approximately three years
2 metrics
CMO start date April 6, 2026 Effective date for Vicki Goodman as Chief Medical Officer
Current CMO tenure approximately three years David Mauro transitioning out after about three years in role

Historical Context

5 past events · Latest: Feb 25 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Feb 25 Earnings and update Positive +6.8% Fourth-quarter and full-year 2025 results with strong cash and AI validation.
Feb 23 Tech conference feature Neutral -0.3% Participation in NVIDIA GTC lightning talk on AI-driven lab and data systems.
Feb 23 Investor conferences Neutral -0.3% Planned appearances at multiple March 2026 healthcare investor conferences.
Feb 18 Earnings date notice Neutral +2.0% Announcement of timing and format for the February 25 earnings call.
Feb 12 Equity inducement grants Negative -3.5% Grant of 820,431 inducement RSUs to new employees under 2024 plan.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent news flow shows mostly aligned price reactions: positive earnings and business updates saw gains, while equity-related grants produced modest pressure, indicating the stock often trades directionally with the perceived quality of news.

Recent Company History

Over the last few months, Recursion highlighted earnings strength and platform progress. On Feb 25, earnings and a strong cash position coincided with a 6.8% gain. Conference and event announcements on Feb 23 and Feb 18 generated small moves. An inducement equity grant on Feb 12 saw a -3.5% reaction. Today’s leadership update fits into an active cadence of strategic and organizational disclosures.

Key Terms

cytokine, pharmacovigilance, biometrics, pembrolizumab, +3 more
7 terms
cytokine medical
"advanced a portfolio of novel cytokine assets."
Small proteins produced by cells that act as chemical messengers to coordinate immune and inflammatory responses, like text messages or traffic signals telling cells when to activate, calm down, or move. Investors care because cytokines are common drug targets and biomarkers; changes in cytokine activity can determine a therapy’s effectiveness, safety, regulatory approval, and market potential, so trial results or safety signals tied to cytokines often drive stock moves.
pharmacovigilance medical
"oversaw early- and late-stage clinical development, regulatory affairs, pharmacovigilance, and biometrics"
Pharmacovigilance is the process of monitoring and assessing the safety of medicines after they are on the market, ensuring that any side effects or risks are identified and managed. For investors, it matters because it helps ensure that pharmaceutical companies maintain safe products, which can influence a company’s reputation, regulatory approval, and financial stability over time.
biometrics medical
"regulatory affairs, pharmacovigilance, and biometrics across a multi-asset pipeline."
Biometrics are measurable physical or behavioral traits—like fingerprints, facial features, voice patterns, heart rate or gait—that uniquely identify or monitor a person, similar to how a key or signature proves identity. Investors care because biometric technology drives products and services in security, payments and health monitoring, affecting revenue opportunities, adoption trends and regulatory or privacy risks that can influence a company’s value and future growth.
pembrolizumab medical
"including KEYTRUDA® (pembrolizumab), across a broad range of tumor types."
A cancer immunotherapy drug that helps the body’s immune system recognize and attack tumor cells by blocking a molecular “brake” that tumors use to hide. Investors watch it because regulatory approvals, clinical trial results, dosing rules, and competition directly affect potential sales, profit forecasts, and the valuation of companies that sell or license the drug—think of trial outcomes as checkpoint signs that can open or close a revenue road.
nivolumab medical
"led cross-functional development for OPDIVO® (nivolumab) and YERVOY®"
A prescription cancer drug that helps the body's immune system spot and attack tumors by blocking a molecular “brake” on immune cells, allowing them to act more aggressively against cancer. Investors monitor it because clinical trial results, regulatory approvals, new uses, or competition can drive significant changes in a drug maker’s sales forecasts, valuation and long-term growth prospects—similar to how a key product launch can reshape a company’s future.
ipilimumab medical
"OPDIVO® (nivolumab) and YERVOY® (ipilimumab) in melanoma and genitourinary cancers."
Ipilimumab is a type of cancer drug that helps the body’s immune system attack tumors by removing a chemical “brake” that normally keeps immune cells from overreacting. For investors, it matters because clinical trial results, regulatory approvals, safety issues, or changes in how broadly it can be used directly affect sales forecasts, competitive positioning, and the valuation of companies involved in developing or selling immune‑based cancer therapies.
U.S. Food and Drug Administration regulatory
"she began her career as a Medical Officer in the U.S. Food and Drug Administration"
The U.S. Food and Drug Administration is the federal agency that evaluates and enforces safety, effectiveness and labeling standards for medicines, medical devices, vaccines, food and related products before they reach consumers. For investors it matters because FDA approvals, warnings or recalls determine whether a product can be sold, how quickly it reaches the market and how costly compliance will be—changes that directly affect a company’s revenue, costs and stock value.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Salt Lake City, UT, March 25, 2026 (GLOBE NEWSWIRE) -- Recursion (Nasdaq: RXRX), a leading clinical-stage TechBio company decoding biology to radically improve lives, today announced that Vicki Goodman, M.D., will become Recursion’s Chief Medical Officer effective April 6, 2026 as David Mauro, M.D., Ph.D. transitions out of the role.

As Recursion advances its pipeline and prepares for key clinical and regulatory milestones, which are consistent with previously communicated expectations, Dr. Goodman brings a rare and differentiated perspective of how to translate scientific promise into successful clinical programs. Her experience spans executive roles in biotech and large pharma, with particular expertise in oncology, as well as experience in clinical practice and as an FDA reviewer.

“We are very excited to welcome Dr. Goodman to Recursion. Vicki's depth of clinical development experience, sound judgment, and the clarity with which she approaches advancing programs through critical regulatory and clinical inflection points are the leadership skills that will help us advance our clinical pipeline,” said Najat Khan, Ph.D., CEO and President of Recursion. “This combination of experience, especially at the later stages of clinical development, will be invaluable as we translate scientific insight into disciplined, high-quality programs and deliver differentiated medicines for patients.”

“Recursion stands apart in the industry through its ambitious integration of scientific and technological rigor to reimagine how medicines are discovered and developed through the power of AI,” said Dr. Goodman. “I’m thrilled to join the company at such an important moment. I look forward to working with Najat, the leadership team, and the broader organization to advance the pipeline, support smart and disciplined development decisions, and help bring impactful new therapies to patients.”

Dr. Goodman is a seasoned physician executive with more than two decades of experience in oncology drug development and medical leadership. Most recently, she served as Chief Medical Officer of Mural Oncology, where she built and led the development organization and advanced a portfolio of novel cytokine assets. Previously, she was Executive Vice President, Product Development and Medical Affairs and Chief Medical Officer at Exelixis, where she oversaw early- and late-stage clinical development, regulatory affairs, pharmacovigilance, and biometrics across a multi-asset pipeline.

She has held senior oncology leadership roles at Merck, where she served as Vice President of Clinical Research and Therapeutic Area Head of Late-Stage Oncology, overseeing key elements of the company’s late-stage portfolio, including KEYTRUDA® (pembrolizumab), across a broad range of tumor types. Prior to that, at Bristol Myers Squibb, she was a member of the Oncology Senior Leadership Team and led cross-functional development for OPDIVO® (nivolumab) and YERVOY® (ipilimumab) in melanoma and genitourinary cancers.

Earlier in her career at GlaxoSmithKline, Dr. Goodman led development of dabrafenib from early clinical expansion through regulatory approval, and contributed to the advancement of multiple oncology assets entering clinical development. 

Before she began her career as a Medical Officer in the U.S. Food and Drug Administration, Dr. Goodman received her M.D. from Albert Einstein College of Medicine and completed her clinical training in internal medicine and hematology/oncology at the University of Michigan.

Concurrently, Recursion’s current CMO, David Mauro, M.D., Ph.D. will be transitioning from his role after approximately three years.

“Recursion has been a remarkable place to serve, and I’m proud of what we’ve built together over the past several years,” said Dr. Mauro. “I’m especially grateful to my colleagues across clinical development and the broader organization for their collaboration and commitment to patients. I believe Recursion is uniquely positioned at the intersection of technology and drug development, and I look forward to watching the continued progression of the pipeline to potential treatments for patients in the years ahead.”

“On behalf of everyone at Recursion, I want to thank Dr. Mauro for his leadership, partnership, and many contributions to our clinical organization and pipeline,” said Najat Khan, Ph.D., CEO and President of Recursion. “Since joining Recursion, David has helped strengthen our medical organization, guided the advancement of our clinical portfolio, and supported important milestones across our programs, including the continued progression of REC-4881. We are grateful for his dedication to our mission.”

About Recursion
Recursion (NASDAQ: RXRX) is a clinical-stage TechBio company decoding biology to radically improve lives. Recursion is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline in oncology, rare disease, neuroscience, immunology, and other therapeutic areas with significant unmet need. Enabling its mission is the Recursion OS, an AI-native, end-to-end drug discovery and development platform integrating biology, chemistry, and clinical development into a unified intelligence system. Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter — faster, better, and at scale — for patients who are waiting.

Recursion’s platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire, where its automated biology and chemistry laboratories generate proprietary data at industrial scale. Recursion also maintains offices in New York, Montréal, and London, three global hubs for talent and leadership at the intersection of AI and scientific innovation. Learn more at www.recursion.com, or connect on X and LinkedIn.



Investor Contact
investor@recursion.com

Media Contact
media@recursion.com

FAQ

Who is Recursion (RXRX) appointing as Chief Medical Officer and when does it start?

Recursion is appointing Vicki Goodman, M.D. as CMO effective April 6, 2026. According to the company, she brings decades of oncology drug‑development and FDA review experience to lead clinical programs.

What does the RXRX CMO change mean for Recursion's REC‑4881 program?

The CMO change does not stop REC‑4881 progression; the company reports continued advancement of the program. According to the company, leadership transition aims to sustain clinical momentum and disciplined development decisions.

Who is leaving the CMO role at Recursion (RXRX) and how long did they serve?

David Mauro, M.D., Ph.D. will transition out of the CMO role after approximately three years. According to the company, he helped strengthen clinical development and supported milestones across the clinical portfolio.

What relevant experience does Vicki Goodman bring to Recursion (RXRX) as CMO?

Dr. Goodman brings more than two decades of oncology drug‑development and medical leadership, including roles at Exelixis, Merck, and FDA experience. According to the company, this background supports late‑stage development and regulatory interactions.

How might the RXRX management change affect investor expectations or clinical timelines?

The appointment signals strengthened clinical leadership but represents an organizational change requiring integration. According to the company, Dr. Goodman’s late‑stage experience is intended to support timely, disciplined advancement of the pipeline.