Full-Time

Senior Advisor

Molecular Pharmacology

Posted on 9/9/2026

Centessa Pharmaceuticals

Centessa Pharmaceuticals

51-200 employees

Clinical-stage pharma with asset-centric model

Compensation Overview

$140k - $215k/yr

+ Annual bonus

Boston, MA, USA

Remote

Remote within the US, with occasional travel.

Bachelor's, Master's, PhD

Category
Biology & Biotech (1)

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Requirements
  • PhD in Neuroscience, Pharmacology, Physiology, or a related field, or an MS/BS with commensurate industry experience.
  • At least 6 years of relevant postdoctoral or industry experience.
  • Demonstrated experience with in vitro functional and affinity modulation of G protein-coupled receptor targets in a drug discovery setting.
  • Expertise in brain slice electrophysiology and related circuit-level approaches, including study design, contract research organization oversight, and data interpretation for drug development decision-making.
  • A strong foundation in molecular and cellular pharmacology.
  • Experience working with contract research organizations and external research partners.
  • Ability to connect mechanistic data to in vivo relevance and program decision-making.
  • Ability to operate collaboratively in a matrixed environment.
Responsibilities
  • Serve as the Molecular Pharmacology team’s subject-matter expert in neuroscience pharmacology, guiding in vitro and ex vivo assay selection, study design, and translational interpretation of results.
  • Own the scientific strategy and design of in vitro and ex vivo pharmacology studies, emphasizing brain slice electrophysiology and circuit-level functional assays executed at contract research organizations.
  • Manage external contract research organizations, including protocol development, technical alignment, data review, and troubleshooting to ensure high-quality, fit-for-purpose studies.
  • Partner with the Director of Molecular Pharmacology and cross-functional colleagues in chemistry, biology, translational, and in vivo functions to interpret results and inform program decisions.
  • Contribute to scientific discussions around program direction, refine hypotheses, and deepen biological understanding.
  • Provide scientific guidance and review to junior team members.
Desired Qualifications
  • Microelectrode array experience.
Centessa Pharmaceuticals

Centessa Pharmaceuticals

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Centessa Pharmaceuticals uses an asset-centric hub-and-spoke model formed from ten subsidiary companies to advance multiple therapies. Its lead program ORX750 is an oral orexin receptor 2 agonist for sleep-wake disorders and is in Phase 2a with Phase 2 data expected in 2025. It also develops an early-stage immuno-oncology program based on the LockBody technology, which engineers antibodies to improve cancer treatment. The company funds development through equity, debt, and partnerships and aims to move ORX750 toward regulatory approval while expanding its oncology portfolio.

Company Size

51-200

Company Stage

IPO

Headquarters

Boston, Massachusetts

Founded

2021

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Simplify Jobs

Simplify's Take

What believers are saying

  • Nxera announced an $8.6 million milestone from Centessa on September 3, 2026.
  • Lilly completed the acquisition on June 24, 2026, providing global resources.
  • Takeda’s oveporexton FDA review in Q3 2026 expands orexin market credibility.

What critics are saying

  • Takeda’s oveporexton leads Centessa in Phase 3 and FDA review, compressing first-mover advantage.
  • Centessa generated zero product revenue in Q1 2026; commercialization remains unproven.
  • Lilly can deprioritize ORX142 and ORX489 post-close, shrinking Centessa’s standalone identity.

What makes Centessa Pharmaceuticals unique

  • Lilly’s June 24, 2026 acquisition validates Centessa’s orexin portfolio and science.
  • Cleminorexton/ORX750 targets OX2R directly, a mechanistic sleep-wake switch.
  • Nxera-originated ORX142 and ORX489 extend the platform beyond narcolepsy.

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Benefits

Remote Work Options

Flexible Work Hours

Wellness Program

Mental Health Support

Stock Options

Company Equity

Conference Attendance Budget

Professional Development Budget

Telework isn't listed but Remote Work Options covers it

Phone/Internet Stipend

Home Office Stipend

Growth & Insights and Company News

Headcount

6 month growth

-2%

1 year growth

-1%

2 year growth

-5%
Associated Press
Sep 3rd, 2026
Nxera Pharma secures $8.6M milestone payment from Centessa following late-stage development progress

Nxera Pharma will receive an $8.6 million milestone payment from Centessa Pharmaceuticals following late-stage development progress on Centessa's selective orexin receptor 2 agonist portfolio. The payment stems from Nxera's research collaboration with Centessa and will be recognised as revenue in Q3 2026. Centessa, now a wholly-owned subsidiary of Eli Lilly following Lilly's acquisition completed in June 2026, achieved the development milestone with its clinical-stage molecules designed to treat diseases associated with sleep-wake regulation and neurological disorders. Nxera retains rights to future development and commercialisation milestones, as well as royalties, related to the programmes. Christopher Cargill, president and CEO of Nxera Pharma, said the portfolio has great potential to address major unmet needs across a broad range of disorders.

American Academy of Sleep Medicine
Jul 19th, 2026
Talking sleep | live from SLEEP 2026.

Talking sleep | live from SLEEP 2026. Season 8 | episode 12. In this special live episode recorded from the SLEEP 2026 annual meeting in Baltimore, host Dr. Seema Khosla welcomes Dr. Sanjay Patel, director of the clinical sleep program at University of Pittsburgh Medical Center, to discuss groundbreaking medications for sleep disorders poised for FDA approval in 2026 and 2027. The pharmaceutical landscape for sleep medicine is undergoing unprecedented transformation. Dr. Patel surveys the emerging drug pipeline that will fundamentally change how clinicians treat obstructive sleep apnea, narcolepsy, and idiopathic hypersomnia. For obstructive sleep apnea, Dr. Patel discusses AD-109 (atomoxetine and R-oxybutynin), explaining the mechanistic rationale and practical considerations including use with tirzepatide. The Incannex drug combining dronabinol and acetazolamide receives analysis for different patient populations, and sultiame is discussed as a carbonic anhydrase inhibitor option. A critical framework emerges: Should treatment be symptom-based or airway-focused when PAP-intolerant patients present? Tirzepatide, the GLP-1 agonist FDA-approved for moderate-to-severe OSA, receives comprehensive coverage including muscle loss concerns, long-term use, and emerging oral GLP-1 options. Retatrutide, the triple-hormone agent combining GLP-1, GIP, and glucagon, is also discussed. The episode's most exciting segment focuses on orexin agonists for narcolepsy. Three pharmaceutical companies - Alkemeres, Centessa (purchased by Lilly), and Takeda - are developing these mechanistically novel agents. Dr. Patel clarifies how these medications differ, discusses why one medication disrupted nocturnal sleep (suggesting continued roles for oxybates), and addresses how clinicians will choose between similar medications. Dr. Patel emphasizes a fundamental question: Should the field prioritize symptom management versus airway patency for OSA, and mechanistic approaches versus symptom management for narcolepsy? Whether you're interested in emerging OSA treatments, narcolepsy innovations, or the future of pharmacological sleep medicine, this live episode provides essential updates on medications that will soon reshape clinical practice. Join American Academy of Sleep Medicine for this exciting conversation about how sleep medicine will transform in the coming years. Dr. Sanjay R. Patel, an expert in sleep health, is certified in pulmonary disease and sleep medicine by the American Board of Internal Medicine. Dr. Patel is a professor of medicine and epidemiology at University of Pittsburgh, and medical director of UPMC Comprehensive Sleep Disorders program. He earned a master's degree in epidemiology from the Harvard School of Public Health and a medical degree from Harvard Medical School and Massachusetts Institute of Technology. He completed a residency at the University of Pennsylvania Health System and a fellowship at Massachusetts General Hospital. Dr. Patel's research focuses on the health implications of poor sleep with particular interest on the relationships between sleep and cardiometabolic disease. He directs the Center for Sleep and Cardiovascular Outcomes Research at the University of Pittsburgh. He has published extensively on the subject of obesity management and glucose metabolism with sleep apnea, as well as the association between curtailed sleep and long-term health effects.

Genetic Engineering & Biotechnology News
Apr 10th, 2026
Drugs from a text prompt, Wegovy pill competition dampens Lilly's surge.

Drugs from a text prompt, Wegovy pill competition dampens Lilly's surge. April 10, 2026 From designing drugs with a simple text prompt to running experiments guided by extended reality, a new wave of agentic AI is transforming the modern lab. Its editors discuss the latest autonomous systems accelerating biological discovery. In business deals, Gilead Sciences has acquired Tubulis in a transaction worth up to $5 billion, strengthening the buyer's position in antibody-drug conjugates for cancer. Correspondingly, Eli Lilly and Biogen are each making billion-dollar-plus bets, acquiring Centessa, a sleep disorder drug developer, and Apellis, known for its work in immunology and rare diseases. Its episode rounds out by unpacking the dynamic obesity drug market, where intensifying competition from Novo Nordisk's Wegovy pill is prompting Lilly to temper the 2026 sales outlook for its oral obesity drug, Foundayo. Listed below are links to the GEN stories referenced in this episode of Touching Base:

BioSpace
Mar 31st, 2026
Lilly wakes up sleep market with $6.3B Centessa buy to challenge Takeda.

Lilly wakes up sleep market with $6.3B Centessa buy to challenge Takeda. March 31, 2026 | In the buyout, Eli Lilly picks up Centessa Pharmaceuticals' lead asset cleminorexton, which could go toe-to-toe with Takeda's oveporexton, currently under FDA review with a decision expected in the third quarter. Looking to further expand its expertise beyond the cardiometabolic and neurology arenas, Eli Lilly is taking over Centessa Pharmaceuticals and its pipeline of sleep disorder drugs - a move that could put the pharma in direct competition with Takeda. Under the terms of the acquisition agreement, announced Tuesday morning, Lilly will snap up Centessa for $38 per share or $6.3 billion upfront. The pharma has also offered a contingent value right that entitles stockholders to $9 more per share if the deal hits certain milestones, including one of two FDA approvals before a certain period of time lapses. This contingent offer could add $1.5 billion more to the total buyout value. Lilly and Centessa expect to close the transaction in the third quarter of 2026. The boards of directors of both companies have approved the deal. At the heart of the acquisition agreement is Centessa's lead asset cleminorexton, an oral orexin receptor 2 (OX2R) agonist being trialed for narcolepsy type 1, narcolepsy type 2 and idiopathic hypersomnia. Orexin is a key neuropeptide that regulates the sleep-wake cycle, according to the biotech's website, in turn promoting wakefulness. Drugs that activate this pathway could help address excessive daytime sleepiness as well as improve attention, cognition and fatigue. In April 2025, Centessa released Phase 1 data showing that a 5-mg oral dose of cleminorexton delayed sleep by an average of 37.9 minutes compared to 15.3 minutes in placebo recipients, resulting in a "statistically significant" treatment effect of 22.6 minutes, the biotech said at the time. This readout "reinforces ORX750 as a potentially best-in-class OX2R agonist relative to competitors," Leerink analysts wrote an April 7, 2025 note. Analysts at BMO Capital Markets said Centessa's orexin receptor agonist has "best-in-class" potential for narcolepsy, putting the company in a strong position in the $15 billion market. April 7, 2025 With the Centessa pickup, Lilly will go toe-to-toe with Takeda, which is far ahead in the narcolepsy race with its late-stage oveporexton, also an OX2R agonist. In July 2025, Takeda announced that oveporexton significantly improved excessive daytime sleepiness, attention, quality of life, functioning and cataplexy in two Phase 3 studies. The FDA accepted Takeda's approval submission for the candidate last month, with a decision out in the third quarter of this year. Also in the narcolepsy game is Alkermes, which in November last year announced that its own OX2R agonist alixorexton aced Phase 2 and would move into late-stage development. The drug improved wakefulness and eased daytime sleepiness in patients with narcolepsy type 2, according to results presented at the time. Alixorexton's Phase II performance sets it up for late-stage success, according to analysts at Truist Securities. Alkermes expects to launch a global late-stage program early next year for narcolepsy type 2. November 13, 2025 Aside from cleminorexton, Lilly will also come into possession of Centessa's broader pipeline of OX2R agonists, which includes additional preclinical assets with therapeutic potential "across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions," the pharma said Tuesday. Tristan is BioSpace 's senior staff writer. Based in Metro Manila, Tristan has more than eight years of experience writing about medicine, biotech and science. He can be reached at [email protected], [email protected] or on LinkedIn.

PR Newswire
Mar 31st, 2026
Lilly to acquire Centessa for $6.3B to advance sleep-wake disorder treatments

Eli Lilly has agreed to acquire Centessa Pharmaceuticals for $38.00 per share in cash plus contingent value rights worth up to $9.00 per share, valuing the deal at approximately $6.3 billion upfront with potential additional payments of $1.5 billion. The upfront consideration represents a 40.5% premium to Centessa's 30-day volume-weighted average share price. Centessa is developing orexin receptor 2 agonists for sleep-wake disorders, with lead candidate cleminorexton showing promising results in Phase 2a studies across narcolepsy type 1, narcolepsy type 2 and idiopathic hypersomnia. The acquisition expands Lilly's neuroscience portfolio into sleep medicine. Contingent payments are tied to FDA approvals of cleminorexton or ORX142 by 2030. The transaction, structured as a scheme of arrangement, requires shareholder approval and is expected to close in the third quarter.