Full-Time

Senior Manager

Global Publications

Mirum Pharmaceuticals

Mirum Pharmaceuticals

201-500 employees

ASBT inhibitors for rare liver diseases

Compensation Overview

$170k - $190k/yr

Foster City, CA, USA

Hybrid

Hybrid role; approximately 30% travel, including US and international travel.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Word/Pages/Docs
Excel/Numbers/Sheets

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Requirements
  • An advanced degree and at least 3 years of experience in scientific communication, training, and/or publications planning and development in an agency or pharmaceutical environment, or applicable pharmaceutical experience with transferable skills.
  • Strong project management skills and the ability to negotiate and facilitate alignment among internal and external stakeholders, including key opinion leaders, authors, and cross-functional teams.
  • Experience working with cross-functional stakeholders and/or agencies to develop abstracts, posters, and oral presentations.
  • Effective interpersonal and communication skills.
  • Ability to stay organized and multitask in a fast-paced, deadline-driven environment.
  • Experience managing vendors and budgets.
  • Advanced computer and Internet skills, including Microsoft Word, PowerPoint, Excel, Veeva RIM, electronic publication management tools such as PubStrat and Datavision, reference databases such as EndNote, and PubMed.
  • Ability to travel approximately 30% of the time in the United States and internationally.
Responsibilities
  • Understand scientific and medical content in the company’s therapeutic areas.
  • Review and edit scientific content for oral and poster presentations at congresses.
  • Manage publication vendors and collaborate with key internal and external stakeholders.
  • Implement the publication management system.
  • Develop scientific training tactics, including internal medical science liaison training decks, tools, and frequently asked questions.
  • Engage internal and external subject matter experts, when appropriate, in scientific communication tactics and content development.
  • Manage and contribute to global publication and scientific communications plans for company needs.
  • Work with Medical Communications and Publications agencies on publication strategies and deliverables.
  • Apply therapeutic-area data knowledge to scientific publishing projects focused on congress presentations.
  • Execute activities within agreed timelines for preparing medical, scientific, and health economics abstracts, posters, and oral presentations.
  • Assist with Medical Legal and Regulatory Committee review and approvals as appropriate.
  • Interface with external experts, including physicians and other health care professionals, and collaborate with Clinical Research and Development, Compliance, Safety, Biostatistics, Clinical Operations, and Commercial stakeholders to ensure accurate and timely information delivery, address conflicting demands, and review scientific presentations and training programs.
Mirum Pharmaceuticals

Mirum Pharmaceuticals

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Mirum Pharmaceuticals develops and commercializes therapies for rare liver diseases. Its lead drug LIVMARLI (maralixibat) is an oral ASBT inhibitor that lowers bile acid buildup to relieve itching in cholestatic conditions such as Alagille syndrome, and the company is pursuing LIVMARLI for additional rare liver diseases, with volixibat as another ASBT inhibitor in its pipeline. The company differentiates itself by focusing on rare pediatric and adult cholestatic diseases and building dedicated commercialization infrastructure in the U.S. and other major markets, including partnerships with physicians, payers, and patient groups to improve patient access. Mirum’s goal is to bring effective therapies to patients with rare bile-duct and liver disorders, expand LIVMARLI indications, and establish a sustainable market presence in key markets.

Company Size

201-500

Company Stage

IPO

Headquarters

Foster City, California

Founded

2018

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 net product sales reached $176.2 million, and guidance rose to $680–700 million.
  • FDA granted volixibat Breakthrough Therapy and Orphan Drug designations in August 2026.
  • Brelovitug and volixibat posted positive Phase 2b data, creating multiple 2026–2027 catalysts.

What critics are saying

  • FDA recommended an extra volixibat Phase 3 study in August 2026, delaying PSC filing to H1 2027.
  • Zilurgisertib depends on a September 26, 2026 PDUFA; rejection crushes Mirum’s growth narrative.
  • Mirum’s revenue concentration in LIVMARLI and bile-acid medicines exposes it to payer pressure and competitive erosion.

What makes Mirum Pharmaceuticals unique

  • Mirum dominates rare pediatric cholestasis with LIVMARLI and U.S. commercial infrastructure.
  • Mirum pairs approved liver drugs with a late-stage rare-disease pipeline and regulatory assets.
  • Mirum licensed zilurgisertib from Incyte; FDA accepted the NDA for September 26, 2026.

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Benefits

Hybrid Work Options

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

1%
CNBC TV18
Aug 20th, 2026
US FDA approves Regeneron's rare bone disorder drug.

US FDA approves Regeneron's rare bone disorder drug. Regeneron's Pasatru has received US FDA approval for adults with FOP after clinical trials showed a significant reduction in abnormal bone formation. By Reuters August 20, 2026, 8:59:40 AM IST (Published) The US FDA on Wednesday (August 19) approved Regeneron's drug for a rare genetic disorder after it significantly reduced abnormal bone formation in certain soft tissues. New York-based Regeneron's shares rose 4%. The drug, garetosmab, branded as Pasatru, was approved to treat adults with fibrodysplasia ossificans progressiva (FOP) - a condition in which muscle, tendon and ligament tissue gradually turns into bone, leading to a "second skeleton" that causes progressive loss of mobility and reduced life expectancy. In a 56-week trial involving 63 participants, Pasatru reduced the development of new bone abnormalities by 94% in patients treated with a 3 mg per kg dose and by 90% in those given a 10 mg per kg dose, compared with a placebo. The drug works by blocking Activin A, a protein involved in triggering abnormal bone growth in patients with FOP. Susan Rhee, a member of Regeneron's clinical team, told Reuters last week that the company plans to start a trial for children later this year. The drug will compete with French drugmaker Ipsen's oral treatment Sohonos, which in 2023 became the only other treatment approved by the US Food and Drug Administration. Incyte and partner Mirum Pharma, as well as privately held Ashibio, are also developing treatments for the condition. In 2020, Regeneron paused dosing in a mid-stage trial of the drug after five patient deaths, ultimately discontinuing the study and working with global regulators to design the late-stage trial, according to the company. The condition affects roughly 1 in 2 million people worldwide, with around 800 to 900 active diagnosed cases globally, according to data from the National Institutes of Health.

Yahoo Finance
Aug 6th, 2026
FDA requests Phase 3 trial for Mirum's Volixibat, delaying NDA until H1 2027 — MIRM stock crashes 15%

Mirum Pharmaceuticals shares plunged 15% on Thursday after the FDA recommended an additional Phase 3 study for its liver disease candidate Volixibat, potentially delaying the new drug application until the first half of 2027. Citizens lowered its price target to $137 from $146 whilst maintaining an Outperform rating. The regulatory setback overshadowed strong second-quarter results. Mirum reported revenue of $176.2 million, beating analysts' estimates of $167.3 million. The company raised its full-year net product sales guidance to $680 million to $700 million, from $660 million to $680 million. Mirum ended the quarter with $561.3 million in cash and equivalents. Volixibat has already received FDA Breakthrough Therapy and Orphan Drug designations.

Yahoo Finance
Aug 6th, 2026
Mirum raises 2026 guidance to $700M, delays PSC drug filing amid FDA review

Mirum Pharmaceuticals raised its full-year 2026 net product sales guidance to $680 million to $700 million, citing growth in Alagille syndrome and expanding adult PFIC diagnosis. The company secured $690 million through a convertible note offering, improving its capital structure whilst settling 75% of 2029 notes. The firm identified a significant opportunity in adult PFIC, estimating at least 2,000 addressable patients each in the US and Europe. Commercial operations achieved a high-50s percent cash contribution margin, representing a 5 percentage point year-over-year improvement. Mirum delayed its volixibat PSC NDA submission due to alignment issues with FDA reviewers but received Breakthrough Therapy Designation. The company targets a first-half 2027 NDA submission for PSC and anticipates Phase III PBC results in Q1 2027.

Yahoo Finance
Aug 6th, 2026
Mirum Pharmaceuticals' Q2 revenue hits $176M, up 38% year-on-year despite widened loss

Mirum Pharmaceuticals reported revenue of $176.24 million for the quarter ended June 2026, up 37.9% year-over-year. The figure exceeded the consensus estimate of $164.76 million by 6.97%. The company posted a loss of $0.80 per share, compared to $0.12 a year ago, slightly missing the estimated loss of $0.77 per share. Product sales showed strong performance across categories. Livmarli generated $128.72 million, surpassing the $119.6 million analyst estimate. Bile acid medicines brought in $47.52 million, also beating expectations of $45.64 million. Despite beating revenue estimates, Mirum's shares fell 18.7% over the past month, underperforming the S&P 500's 3.5% gain.

Investing.com
May 13th, 2026
Mirum prices $600m convertible notes offering due 2032 By Investing.com

Mirum prices $600m convertible notes offering due 2032