B

Biogen

Develops therapies for neurological disorders

External Stakeholder Engagement Senior Analyst - External Stakeholder Engagement

Full-TimeUpdated on 10/23/2026
No salary listed
Senior
Bachelor's
Shanghai, China
In PersonOn-campus in Shanghai.
Business & StrategyBusiness Operations

About the job

Requirements
  • A university degree or an equivalent combination of education and experience is required.
  • More than 5 years of experience in a fast-paced administration or operational role is required.
  • Expanded conceptual knowledge in the job discipline and broadened capabilities are required.
  • Excellent verbal and written communication skills in Korean and English are required.
  • Experience partnering and collaborating with cross-functional teams is required.
  • Strong customer service and organizational skills, and experience managing a process, are required.
  • Experience working with workflow programs and strong overall proficiency with Microsoft Office tools are required.
  • Ability to accomplish multiple tasks within agreed timeframes by effectively prioritizing duties in a fast-paced environment is required.
Responsibilities
  • Perform structured work assignments related to the job discipline and use existing procedures and guidelines to solve routine problems.
  • Support the Engagement Owner with the end-to-end process in the ESE tool, from engagement submission through closure, providing operational guidance and administrative support for on-time execution.
  • Support the Sponsorship Owner with the end-to-end process in the SGG tool, from sponsorship request submission through closure, providing operational guidance and administrative support for on-time execution.
  • Serve as the subject matter expert and primary contact for Biogen engagement and sponsorship owners and other employees involved in ESE and SGG processes; support Affiliate teams with submissions, international colleagues with cross-border engagements, and back-office execution.
  • Maintain electronic records, follow up on outstanding items, and ensure timely completion of transactions.
  • Resolve straightforward problems by analyzing possible solutions using technical experience, judgment, and precedents, while operating within clear guidelines.
  • Seek guidance from more senior roles in non-standard situations.
  • Explain factual, sometimes complex information to others in straightforward situations.
  • Maintain GBS process documentation, including work instructions, job aids, and quick cards, and train new joiners.
  • Conduct routine operational meetings with internal business partners.
  • Report and monitor KPIs and metrics for ESE and Sponsorship processes in line with established SLAs.
  • Report and analyze root causes of incidents related to ESE and Sponsorship processes, and propose and implement mitigation actions.
  • Support continuous improvement of ESE and Sponsorship processes.
  • Support the transition of ESE and Sponsorship processes from other markets into GBS.
  • Provide support or backup to other countries transitioned to GBS in processing ESE and Sponsorship requests.
Desired Qualifications
  • Experience working in Pharma or Biotech is a plus.
  • Knowledge of external stakeholder engagement and sponsorship processes and related regulations is a plus.
  • Knowledge of event management is a plus.

About the company

B

Biogen

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Website

Biogen is a global biotechnology company focused on neuroscience. It discovers, develops, and delivers therapies for neurological disorders, such as multiple sclerosis and other neurodegenerative diseases. Its product process starts with research and development to identify potential drugs, followed by clinical testing and regulatory approval, ultimately leading to commercialization and patient treatment. Biogen differentiates itself through a long history (founded in 1978), a deep specialization in neuroscience, and an integrated pipeline that moves ideas from discovery to approved medicines, aiming to create value for shareholders while helping communities. The company’s goal is to advance therapies for neurological diseases to improve patients’ lives and generate sustainable value for stakeholders.

Company Size

5,001-10,000

Company Stage

IPO

Headquarters

Cambridge, Massachusetts

Founded

1978

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Simplify's Take

What believers are saying

  • LEQEMBI Pen won Japan approval on September 16, 2026, expanding at-home dosing.
  • China approved LEQEMBI subcutaneous initiation on September 3, 2026, accelerating access.
  • Apellis closed on May 14, 2026, adding SYFOVRE and EMPAVELI revenue.

What critics are saying

  • Biogen halted BIIB122 after May 21, 2026 Phase 2b failure in Parkinson’s disease.
  • Genentech won $124.3 million against Biogen in November 2025; appeal remains pending.
  • TECFIDERA exclusivity expired, generics spread, and 1,400 layoffs expose franchise erosion.

What makes Biogen unique

  • Biogen pairs neuroscience depth with marketed Alzheimer’s, MS, and rare-disease franchises.
  • Eisai-Biogen launched LEQEMBI IQLIK in the U.S. on August 24, 2026.
  • Biogen and Stoke advanced zorevunersen into Phase 3 EMPEROR for Dravet syndrome.

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Benefits

  • Remote Work Options
  • Professional Development Budget

Growth & Insights and Company News

6 month growth

-10%

1 year growth

-10%

2 year growth

-10%
Yahoo Finance
Oct 22nd, 2026
Biogen shares rise 5% as BofA lifts price target to $244 ahead of a "quiet" Q3

Biogen shares rose 5% after BofA raised its price target to $244 from $219 and kept a Neutral rating. The bank expects a "relatively quiet" third quarter. TD Cowen also lifted its target to $250 from $225 a day earlier. The stock now trades above both targets. The consensus target has climbed 43% in a year to $247, and the forward price-to-earnings ratio is near its five-year high of about 20. Second-quarter revenue rose 3% to $2.7 billion. Analysts expect about 6% growth this year and 2% to 3% a year through 2028. Biogen reports third-quarter results on October 28. It has warned that charges of $290 million to $320 million will cut earnings per share by $1.75 to $1.95.

Biotech Today
Oct 17th, 2026
City Therapeutics raises $200M for RNAi beyond the liver.

City Therapeutics raises $200M for RNAi beyond the liver. City Therapeutics' $200 million IPO backs RNAi development beyond the liver, with an anticoagulant contender and partnerships in eye and brain diseases. Key facts. * IPO proceeds: City Therapeutics raised $200 million in an upsized initial public offering. * Lead therapy: An RNA interference candidate could become an alternative to blockbuster-selling anticoagulants. * Eye-disease partnership: City Therapeutics has a partnership with Bausch + Lomb in eye diseases. * Central nervous system partnership: City Therapeutics has a partnership with Biogen in central nervous system disorders. City Therapeutics raised $200 million in an upsized initial public offering to advance RNA interference medicines, including a platform aimed at reaching tissues beyond the liver. City Therapeutics has raised $200 million in an upsized initial public offering, securing capital for a drug-development strategy that reaches beyond the liver, an important destination for RNA interference medicines. Its investment case combines a lead therapy that could offer an alternative to established anticoagulants with technology intended to deliver gene-silencing drugs to other tissues. The financing addresses a central challenge in biotechnology: turning a promising way of intervening in disease into medicines that can reach the right cells safely and reliably. City also has partnerships with Bausch + Lomb in eye diseases and Biogen in central nervous system disorders. Those relationships give the platform a broader development footprint, but they do not establish that its experimental treatments will work. More capital, but no shortcut to clinical evidence. The upsized offering raised $200 million, according to MedCity News. The financing gives City resources to pursue its pipeline and delivery technology. It does not, on its own, resolve the scientific and clinical risks that will determine their value. The distinction matters because an IPO measures a company's ability to secure funding, not the effectiveness of its medicines. A larger offering can support development work, but investors still need evidence that a treatment produces its intended biological effect and that the effect translates into a benefit for patients. The supplied offering details do not establish a share price, valuation, net proceeds after expenses or a program-by-program spending plan. Without those terms, the amount raised cannot support a precise judgment about dilution, cash runway or how much capital will reach any particular therapy. The sounder focus is what evidence the financing may help City generate. Why delivery beyond the liver matters. RNA interference, or RNAi, is a way to reduce production of a selected protein by targeting the molecular instructions used to make it. Rather than directly blocking a protein after it has been produced, an RNAi medicine seeks to interrupt the process upstream. Its therapeutic usefulness depends on choosing a suitable target and delivering the treatment to the cells that matter. Delivery is therefore part of the medicine's core design, not merely a packaging problem. A treatment must reach the relevant tissue, enter the appropriate cells and remain active long enough to produce a useful effect. Success at silencing a target in one setting does not automatically establish that the same approach will succeed elsewhere in the body. For City, expansion beyond the liver could widen the range of diseases its technology can address. But that opportunity also sets a demanding standard of proof. Investors will need to distinguish evidence that a drug reaches a tissue from evidence that it changes the course of disease. Both are important, and neither should be assumed from the platform's ambition. The anticoagulant opportunity rests on patient benefit. City's lead RNAi therapy could become an alternative to blockbuster-selling anticoagulants. That places the program against an established treatment category rather than a market with no existing options. The commercial opportunity is meaningful in principle, but the description of a potential alternative is not evidence of superiority. City's lead RNAi therapy could become an alternative to blockbuster-selling anticoagulants. Anticoagulants reduce the blood's ability to form clots. Their clinical use involves balancing protection against harmful clotting with the risk of bleeding. Any new approach seeking a role in that treatment landscape must demonstrate a useful balance of benefit and risk in the patients for whom it is intended. For an RNAi candidate, the connection between gene silencing and patient outcomes will be central. Showing that a target has been suppressed is different from showing that patients experience fewer harmful events or an acceptable safety profile. Duration of action and the ability to manage treatment around changing medical needs would also be relevant questions, rather than advantages investors should presume. The available facts do not identify the lead therapy's target, trial stage, dosing schedule or clinical results. They therefore support an opportunity to investigate, not a forecast that City will displace existing medicines. Partnerships broaden the platform's reach. The Bausch + Lomb and Biogen partnerships extend City's work into eye diseases and central nervous system disorders, respectively. They provide concrete examples of how the company's RNAi design and delivery technology is being pursued outside its lead program. These relationships matter because a platform business depends on more than the prospects of an individual drug. If technology can support useful medicines across distinct tissues and diseases, it may create additional development opportunities. Conversely, a result in one program may say little about another when the target cells, delivery requirements and disease biology differ. The partnerships should not be treated as interchangeable proof points. Work in eye disease cannot by itself validate a treatment for a central nervous system disorder, and neither establishes the clinical prospects of the anticoagulant alternative. No partnership payments, milestone amounts or royalty terms are supplied. Investors consequently cannot use these relationships to calculate a dependable stream of future cash. Their demonstrated significance here is the breadth of the development relationships, not a quantifiable contribution to revenue. What investors should watch after the IPO. The next useful disclosures would connect City's financing to a clear development plan: which programs it intends to prioritize, what studies are designed to establish and how spending is divided between individual candidates and the delivery platform. Those details would help investors judge whether the company is pursuing a focused set of testable objectives. For the lead therapy, attention should fall on clinical evidence relevant to anticoagulant use, rather than molecular activity alone. For the broader platform, the important question is whether delivery outside the liver can produce reproducible, therapeutically useful results without unacceptable safety costs. City's $200 million IPO provides capital to pursue those questions. Its partnerships broaden the scope of the effort, while the lead program gives investors a specific potential commercial application to assess. The financing is a consequential step, but the investment case ultimately depends on what the company can demonstrate with that capital - not simply how much it raised. Frequently asked questions. How much did City Therapeutics raise in its IPO? City Therapeutics raised $200 million in an upsized initial public offering. The financing supports a company developing RNA interference medicines and technology intended to reach tissues beyond the liver. The available facts do not specify the offering's share price, valuation, net proceeds after expenses or allocation of funding among programs. What is RNA interference? RNA interference, or RNAi, reduces production of a selected protein by targeting the molecular instructions used to make it. For a treatment to work, it must reach the appropriate cells and produce a useful biological effect. Successful target suppression must then translate into meaningful patient benefit with an acceptable safety profile. Why is City Therapeutics pursuing RNAi beyond the liver? Reaching tissues beyond the liver could allow City Therapeutics to pursue a broader range of diseases. Delivery is a central challenge because an RNAi medicine must enter the relevant cells to act. Evidence of delivery is important, but it does not by itself establish that a treatment improves patient outcomes. What is the opportunity for City's lead therapy? City Therapeutics' lead RNAi therapy could become an alternative to blockbuster-selling anticoagulants. That creates a potential opportunity in an established treatment category, but does not demonstrate an advantage over existing medicines. The supplied facts do not identify the candidate's target, clinical stage, dosing schedule or results. Which companies have partnerships with City Therapeutics? City Therapeutics has partnerships with Bausch + Lomb in eye diseases and Biogen in central nervous system disorders. These relationships broaden the applications being pursued with its technology. They do not establish clinical success, and the supplied facts contain no payments, milestones or royalty terms from which to estimate future revenue. What should investors watch following the IPO? Investors should watch for program priorities, spending plans and evidence connecting RNAi activity to patient benefit. For the lead therapy, efficacy and safety relevant to anticoagulant use will matter. For the broader platform, the central question is whether delivery beyond the liver produces reproducible, therapeutically useful results.

BioSpace
Oct 15th, 2026
Arrowhead's blood-brain barrier tech is 'arguably better' than others, analysts say after data drop.

Arrowhead's blood-brain barrier tech is 'arguably better' than others, analysts say after data drop. October 15, 2026 | Arrowhead Pharmaceuticals' siRNA candidate achieved "compelling" tau reductions in an early study of healthy volunteers, with a magnitude of effect that seems to outperform other blood-brain barrier platforms, according to Stifel. Arrowhead Pharmaceuticals' investigational gene silencer lowered tau protein levels in an early study, suggesting that the biotech's approach to bypass the blood-brain barrier may be better than competing technologies. The findings "provide important clinical validation" for Arrowhead's platform for targeting the central nervous system through subcutaneously administered drugs, Stifel analysts said in a Wednesday note. Results from the Phase 1/2a study, disclosed Wednesday, showed a 40% average reduction in CSF tau at day 105 in healthy volunteers who were treated with the low 2.1-mg/kg dose of the siRNA candidate, called ARO-MAPT, on days 1, 8 and 15. In those given a 6.4-mg/kg dose on the same days, CSF tau dropped by 69% on average at day 105. Meanwhile, a 12.8-mg/kg dose of ARO-MAPT injected on days 1 and 15 triggered a mean CSF tau reduction of 73% at day 105. The maximum CSF tau reduction reached 85% in the high-dose cohort. The early trial is actively enrolling patients, with a target of 112 participants, including healthy volunteers for the study's first part and patients with early Alzheimer's disease for the second portion. Wednesday's data came from healthy volunteers. As for safety, the primary objective of the Phase 1/2a trial, Arrowhead said that ARO-MAPT was "generally well tolerated." Treatment-emergent adverse events were largely mild, with no serious side effects, deaths or dropouts due to toxicities. The data, while early, could set Arrowhead up to compete against Biogen, analysts say. Both companies are advancing tau-targeting therapies that work by suppressing the expression of the MAPT gene, which codes for the tau protein. "While details are still relatively light, the data looking compelling," Stifel told investors in a note on Wednesday, adding that the interim findings are "arguably better than what we've seen with other BBB platforms." The firm also hinted at a potential competitive edge for Arrowhead's subcutaneous siRNA asset, writing that the CSF tau knockdown "looks better than [Biogen's] BIIB080," an anti-tau antisense oligonucleotide also known as diranersen that is injected directly into the spine. ARO-MAPT, meanwhile, can be delivered via an injection under the skin. Phase 1b data for diranersen published in 2023 showed that, across various dose levels, CSF tau declined by an average of 30% to 49% at eight weeks after the final dose of Biogen's asset. Diranersen's tau-lowering effect persisted through 24 weeks after the last dose, hitting an average tau reduction of up to 56%. The trial enrolled 46 patients with mild Alzheimer's disease, and its primary endpoint was safety; CSF tau was set as a key exploratory outcome. There have been no direct head-to-head studies between ARO-MAPT and diranersen, which prompted Jefferies to be a bit more reserved about comparing the two assets. The firm in a Wednesday note pointed to differences in study populations and dose strengths. In May, Biogen announced that diranersen failed to meet its primary goal of showing a dose-response effect in cognitive and functional outcomes in the Phase 2 CELIA study. Nevertheless, the company detected "robust reductions in tau pathology" that were consistent with the Phase 1b study. Biogen also touted cognitive improvements and slowing of decline, especially in patients who received the lowest dose of diranersen. Based on these efficacy signals, Biogen has decided to push diranersen into registrational development, though the company has yet to specify a timeline for this. Arrowhead is also moving forward with ARO-MAPT, with additional healthy volunteer and Alzheimer's disease data expected next year. Arrowhead is also in talks with health regulators to enable studies in MAPT-associated frontotemporal dementia and progressive supranuclear palsy, according to the Wednesday announcement.

Yahoo Finance
Oct 12th, 2026
Mastercard and ConocoPhillips are buys near 52-week highs, but Biogen is a sell

Investment research site StockStory picked two stocks to buy and one to avoid among companies trading near 52-week highs. It likes Mastercard and ConocoPhillips, and advises selling Biogen. Mastercard trades at $588.84 per share, or 27x forward earnings. Its revenue grew 16.1% a year over five years, and its return on equity is 182%. ConocoPhillips trades at $134.30, or 12.3x forward earnings. Its revenue grew 10.1% a year over ten years, and its revenue stands at $65.28 billion. Biogen trades at $224.63, or 16.5x forward earnings. Its revenue fell 3% a year over five years, and its earnings per share have declined.

Gaya Herald
Sep 28th, 2026
Trigeminal Neuralgia Pipeline Outlook highlights 10+ Companies and 10+ emerging therapies across clinical development stages.

Trigeminal Neuralgia Pipeline Outlook highlights 10+ Companies and 10+ emerging therapies across clinical development stages. September 29 Trigeminal Neuralgia is a chronic neuropathic pain disorder characterized by spontaneous and elicited paroxysms of electric shock-like or stabbing pain in a region of the face, most frequently affecting the distribution of the second (maxillary) or third (mandibular) division of the trigeminal nerve, with the right side of the face affected more often than the left. (Albany, US) September 28, 2026 - DelveInsight's "Trigeminal Neuralgia - Pipeline Insight, 2026" report provides comprehensive insights about 10+ companies and 10+ pipeline drugs in the Trigeminal Neuralgia pipeline landscape, covering clinical and nonclinical stage products, therapeutics assessment by product type, stage, route of administration, and molecule type, as well as inactive pipeline products. Three types of trigeminal neuralgia have been delineated: classical, secondary, and idiopathic, with bilateral trigeminal neuralgia rare and warranting concern about an underlying neurologic or non-neurologic disorder affecting the cranium. Incidence is higher among women than men and increases with age. Key Takeaways from the Trigeminal Neuralgia Pipeline Report * The Trigeminal Neuralgia pipeline includes 10+ key companies developing therapies, with 10+ products spanning Phase III, Phase II, Phase I, preclinical, and discovery stages, along with discontinued and inactive candidates. * Biogen has the most advanced Trigeminal Neuralgia drug candidate in the pipeline, with Vixotrigine (BIIB074) currently in Phase III development. * Vixotrigine is a centrally and peripherally acting small molecule that functions as a voltage- and use-dependent sodium channel blocker, being developed by Biogen for the treatment of Trigeminal Neuralgia. * Rimegepant, developed by Biohaven Pharmaceuticals, is a calcitonin gene-related peptide (CGRP) receptor antagonist in Phase II development for Trigeminal Neuralgia, with a trial initiated in June 2019. * The pipeline includes therapies across multiple stages of development, highlighting continued innovation in neuropathic pain treatment. * Emerging therapies are being developed through diverse mechanisms, including sodium channel blockers and CGRP receptor antagonists. Gain Strategic Insights into the Trigeminal Neuralgia Pipeline Landscape * Explore the complete Trigeminal Neuralgia Pipeline Outlook. * Analyze Phase III, Phase II, Phase I, preclinical, and discovery-stage assets. * Evaluate emerging companies and late-stage pipeline therapies. * Understand therapeutic assessment by product type, route of administration, and molecule type. * Track collaborations, licensing, acquisitions, and other pipeline development activities. Explore detailed pipeline insights and emerging therapies @ Trigeminal Neuralgia Pipeline Insight Report Trigeminal Neuralgia Disease Overview Pain can be triggered by routine acts, including brushing teeth, shaving, touching the face, eating or drinking, speaking, or a breeze on the face. Diagnosis is clinical, based on pain restricted to the territory of one or more divisions of the trigeminal nerve and sudden, intense, very short paroxysms. The anticonvulsant agents carbamazepine and oxcarbazepine have been considered first-choice treatments for control of paroxysmal pain, with gabapentin, pregabalin, and antidepressant agents tried as additional agents. Microvascular decompression is favored as the surgical procedure for cases not responding to medication. Trigeminal Neuralgia Emerging Drugs Analysis The Trigeminal Neuralgia pipeline features multiple emerging therapies targeting neuropathic pain through novel mechanisms and differentiated therapeutic approaches. Phase III Therapy * Vixotrigine (BIIB074): Biogen - A centrally and peripherally acting small molecule voltage- and use-dependent sodium channel blocker. It is currently the most advanced candidate in the Trigeminal Neuralgia pipeline and is being evaluated in Phase III clinical development. Phase II Therapy * Rimegepant: Biohaven Pharmaceuticals - A calcitonin gene-related peptide (CGRP) receptor antagonist currently being evaluated in Phase II development for Trigeminal Neuralgia, with clinical development initiated in June 2019. Further product details on additional pipeline candidates are provided in the full report. Trigeminal Neuralgia Therapeutic Assessment The report provides comprehensive therapeutic assessment of Trigeminal Neuralgia drugs across multiple development and product parameters. Clinical Trial Phases * Late-stage products (Phase III). * Mid-stage products (Phase II). * Early-stage products (Phase I). * Preclinical candidates. * Discovery-stage candidates. * Discontinued and inactive pipeline candidates. Route of Administration * Intravenous. * Subcutaneous. * Oral. * Intramuscular. Molecule Type * Monoclonal antibody. * Small molecule. * Peptide. Product Type * Mono. * Combination. * Mono/Combination. Trigeminal Neuralgia Pipeline Development Landscape The Trigeminal Neuralgia pipeline reflects ongoing innovation across clinical and preclinical development, with multiple companies advancing therapies targeting neuropathic pain through differentiated mechanisms of action. The pipeline spans early discovery through Phase III clinical development and includes both active and inactive candidates, providing insights into the evolving research landscape. Discover Which Companies and Pipeline Therapies Are Advancing Trigeminal Neuralgia Treatment @ Trigeminal Neuralgia Pipeline Insights Scope of the Trigeminal Neuralgia Pipeline Report * Geography Covered: Global. * Coverage: 10+ companies and 10+ pipeline drugs across clinical and nonclinical development stages. * Clinical Stages Covered: Phase III, Phase II, Phase I, preclinical, discovery, inactive, and discontinued products. * Therapeutic Assessment: Product type, clinical stage, route of administration, and molecule type. * Additional Coverage: Collaborations, acquisitions and mergers, licensing, designations, and other product-related development activities. About DelveInsight DelveInsight is a leading healthcare-focused market research and consulting firm that provides actionable market intelligence and strategic insights across the pharmaceutical, biotechnology, and healthcare industries. With expertise in epidemiology forecasting, competitive intelligence, and pipeline analysis, DelveInsight helps organizations make informed business decisions and stay ahead in an evolving healthcare landscape. Media Contact Company Name: DelveInsight Business Research LLP Contact Person: Mehul Malhotra Email: Send Email Phone: 09650213330 Address:A-1 NV 89107 City: delhi State: Indiana Country: United States Website: https://www.delveinsight.com/